Canonical Allele Identifier: CA2684467614

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107694503-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694503A>G , CM000669.2:g.107694503A>G	GRCh38
NC_000007.13:g.107334948A>G , CM000669.1:g.107334948A>G	GRCh37
NC_000007.12:g.107122184A>G	NCBI36
NG_008489.1:g.38869A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1341+23A>G MANE Select	ENSP00000494017.1:n.1341+23A>G
ENST00000644846.1:c.52+23A>G
ENST00000265715.7:c.1341+23A>G	ENSP00000265715.3:n.1341+23A>G
ENST00000460748.1:n.444+23A>G
ENST00000477350.5:n.189-118A>G
ENST00000480841.5:n.190+23A>G
ENST00000497446.5:n.356+23A>G
NM_000441.1:c.1341+23A>G	NP_000432.1:n.1341+23A>G
XM_005250425.1:c.1341+23A>G	XP_005250482.1:n.1341+23A>G
XM_005250425.2:c.1341+23A>G	XP_005250482.1:n.1341+23A>G
XM_017012318.1:c.1264-118A>G	XP_016867807.1:n.1264-118A>G
NM_000441.2:c.1341+23A>G MANE Select	NP_000432.1:n.1341+23A>G