Canonical Allele Identifier: CA368845958
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107350594C>A (hg19) chr7:g.107710149C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710149C>A , CM000669.2:g.107710149C>A GRCh38
NC_000007.13:g.107350594C>A , CM000669.1:g.107350594C>A GRCh37
NC_000007.12:g.107137830C>A NCBI36
NG_008489.1:g.54515C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2185C>A MANE Select ENSP00000494017.1:p.Leu729Ile
ENST00000644846.1:c.841C>A
ENST00000265715.7:c.2185C>A ENSP00000265715.3:p.Leu729Ile
ENST00000492030.2:n.377-6C>A
NM_000441.1:c.2185C>A NP_000432.1:p.Leu729Ile
XM_005250425.1:c.2185C>A XP_005250482.1:p.Leu729Ile
XM_005250425.2:c.2185C>A XP_005250482.1:p.Leu729Ile
XM_017012318.1:c.2107C>A XP_016867807.1:p.Leu703Ile
NM_000441.2:c.2185C>A MANE Select NP_000432.1:p.Leu729Ile
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