Canonical Allele Identifier: CA2684467597

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107694375-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694379del , CM000669.2:g.107694379del	GRCh38
NC_000007.13:g.107334824del , CM000669.1:g.107334824del	GRCh37
NC_000007.12:g.107122060del	NCBI36
NG_008489.1:g.38745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1264-24del MANE Select	ENSP00000494017.1:n.1264-24del
ENST00000265715.7:c.1264-24del	ENSP00000265715.3:n.1264-24del
ENST00000460748.1:n.367-24del
ENST00000477350.5:n.189-242del
ENST00000480841.5:n.113-24del
ENST00000497446.5:n.279-24del
NM_000441.1:c.1264-24del	NP_000432.1:n.1264-24del
XM_005250425.1:c.1264-24del	XP_005250482.1:n.1264-24del
XM_006716025.2:c.*819del	XP_006716088.1:n.*819del
XM_005250425.2:c.1264-24del	XP_005250482.1:n.1264-24del
XM_006716025.3:c.*819del	XP_006716088.1:n.*819del
XM_017012318.1:c.1264-242del	XP_016867807.1:n.1264-242del
NM_000441.2:c.1264-24del MANE Select	NP_000432.1:n.1264-24del