Canonical Allele Identifier: CA1732755362

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791790456
• gnomAD v4: 7-107698114-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107698114A>G , CM000669.2:g.107698114A>G	GRCh38
NC_000007.13:g.107338559A>G , CM000669.1:g.107338559A>G	GRCh37
NC_000007.12:g.107125795A>G	NCBI36
NG_008489.1:g.42480A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1614+3A>G MANE Select	ENSP00000494017.1:n.1614+3A>G
ENST00000644846.1:c.325+3A>G
ENST00000265715.7:c.1614+3A>G	ENSP00000265715.3:n.1614+3A>G
ENST00000477350.5:n.461+3A>G
ENST00000480841.5:n.463+3A>G
NM_000441.1:c.1614+3A>G	NP_000432.1:n.1614+3A>G
XM_005250425.1:c.1614+3A>G	XP_005250482.1:n.1614+3A>G
XM_005250425.2:c.1614+3A>G	XP_005250482.1:n.1614+3A>G
XM_017012318.1:c.1536+3A>G	XP_016867807.1:n.1536+3A>G
NM_000441.2:c.1614+3A>G MANE Select	NP_000432.1:n.1614+3A>G