Canonical Allele Identifier: CA577198954

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1459517861
• gnomAD v2: 7-107342049-C-A
• gnomAD v3: 7-107701604-C-A
• gnomAD v4: 7-107701604-C-A
• MyVariant Identifiers: chr7:g.107342049C>A (hg19) ; chr7:g.107701604C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701604C>A , CM000669.2:g.107701604C>A	GRCh38
NC_000007.13:g.107342049C>A , CM000669.1:g.107342049C>A	GRCh37
NC_000007.12:g.107129285C>A	NCBI36
NG_008489.1:g.45970C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-223C>A MANE Select	ENSP00000494017.1:n.1804-223C>A
ENST00000644846.1:c.515-223C>A
ENST00000265715.7:c.1804-223C>A	ENSP00000265715.3:n.1804-223C>A
ENST00000480841.5:n.653-223C>A
ENST00000492030.2:n.91-223C>A
NM_000441.1:c.1804-223C>A	NP_000432.1:n.1804-223C>A
XM_005250425.1:c.1804-223C>A	XP_005250482.1:n.1804-223C>A
XM_005250425.2:c.1804-223C>A	XP_005250482.1:n.1804-223C>A
XM_017012318.1:c.1726-223C>A	XP_016867807.1:n.1726-223C>A
NM_000441.2:c.1804-223C>A MANE Select	NP_000432.1:n.1804-223C>A