Canonical Allele Identifier: CA398607058
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049346A>C (hg19) chr17:g.18146032A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146032A>C , CM000679.2:g.18146032A>C GRCh38
NC_000017.10:g.18049346A>C , CM000679.1:g.18049346A>C GRCh37
NC_000017.9:g.17990071A>C NCBI36
NG_011634.1:g.42327A>C
NG_011634.2:g.42327A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6434A>C MANE Select ENSP00000495481.1:p.Glu2145Ala
ENST00000205890.9:c.6434A>C ENSP00000205890.5:p.Glu2145Ala
ENST00000578999.1:n.19A>C
ENST00000615845.4:c.6434A>C ENSP00000481642.1:p.Glu2145Ala
NM_016239.3:c.6434A>C NP_057323.3:p.Glu2145Ala
XM_011523917.1:c.6374A>C XP_011522219.1:p.Glu2125Ala
XM_011523918.1:c.6342+32A>C XP_011522220.1:n.6342+32A>C
XM_011523921.1:c.6428A>C XP_011522223.1:p.Glu2143Ala
XR_934037.1:n.7033A>C
XR_934038.1:n.7033A>C
XM_011523918.2:c.6342+32A>C XP_011522220.1:n.6342+32A>C
XM_017024714.2:c.6374A>C XP_016880203.1:p.Glu2125Ala
XM_017024715.2:c.6437A>C XP_016880204.1:p.Glu2146Ala
XM_024450781.1:c.6213+1440A>C XP_024306549.1:n.6213+1440A>C
NM_016239.4:c.6434A>C MANE Select NP_057323.3:p.Glu2145Ala
Search 100 bp 5'
Search 100 bp 3'