Canonical Allele Identifier: CA16044080
Gene: ADGRV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.90015881C>A (hg19) chr5:g.90720064C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90720064C>A , CM000667.2:g.90720064C>A GRCh38
NC_000005.9:g.90015881C>A , CM000667.1:g.90015881C>A GRCh37
NC_000005.8:g.90051637C>A NCBI36
NG_007083.1:g.166265C>A
NG_007083.2:g.195721C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.9464C>A MANE Select ENSP00000384582.2:p.Ala3155Asp
ENST00000639431.1:c.265+43855C>A ENSP00000491057.1:n.265+43855C>A
ENST00000640374.1:n.2608C>A
ENST00000640779.1:c.4193C>A
ENST00000405460.6:c.9464C>A ENSP00000384582.2:p.Ala3155Asp
ENST00000509621.1:c.2161C>A
NM_032119.3:c.9464C>A NP_115495.3:p.Ala3155Asp
NR_003149.1:n.9477C>A
XM_011543675.1:c.9461C>A XP_011541977.1:p.Ala3154Asp
XM_011543676.1:c.9383C>A XP_011541978.1:p.Ala3128Asp
XM_011543677.1:c.6767C>A XP_011541979.1:p.Ala2256Asp
XM_011543678.1:c.9464C>A XP_011541980.1:p.Ala3155Asp
XM_011543679.1:c.9464C>A XP_011541981.1:p.Ala3155Asp
XR_948560.1:n.272-4255G>T
NM_032119.4:c.9464C>A MANE Select NP_115495.3:p.Ala3155Asp
XM_017009963.2:c.9485C>A XP_016865452.1:p.Ala3162Asp
XM_017009964.2:c.9482C>A XP_016865453.1:p.Ala3161Asp
XM_017009965.1:c.9482C>A XP_016865454.1:p.Ala3161Asp
XM_017009966.2:c.9404C>A XP_016865455.1:p.Ala3135Asp
XM_017009967.1:c.9389C>A XP_016865456.1:p.Ala3130Asp
XM_017009968.2:c.9485C>A XP_016865457.1:p.Ala3162Asp
XM_017009969.2:c.9485C>A XP_016865458.1:p.Ala3162Asp
XM_017009970.2:c.9485C>A XP_016865459.1:p.Ala3162Asp
XM_017009971.2:c.9485C>A XP_016865460.1:p.Ala3162Asp
XM_017009972.1:c.2603C>A XP_016865461.1:p.Ala868Asp
XM_017009973.1:c.2582C>A XP_016865462.1:p.Ala861Asp
XM_017009974.2:c.9485C>A XP_016865463.1:p.Ala3162Asp
XR_001742802.1:n.2523-4255G>T
NR_003149.2:n.9480C>A
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