Canonical Allele Identifier: CA2684468961

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107701699-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701703_107701704del , CM000669.2:g.107701703_107701704del	GRCh38
NC_000007.13:g.107342148_107342149del , CM000669.1:g.107342148_107342149del	GRCh37
NC_000007.12:g.107129384_107129385del	NCBI36
NG_008489.1:g.46069_46070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-124_1804-123del MANE Select	ENSP00000494017.1:n.1804-124_1804-123del
ENST00000644846.1:c.515-124_515-123del
ENST00000265715.7:c.1804-124_1804-123del	ENSP00000265715.3:n.1804-124_1804-123del
ENST00000480841.5:n.653-124_653-123del
ENST00000492030.2:n.91-124_91-123del
NM_000441.1:c.1804-124_1804-123del	NP_000432.1:n.1804-124_1804-123del
XM_005250425.1:c.1804-124_1804-123del	XP_005250482.1:n.1804-124_1804-123del
XM_005250425.2:c.1804-124_1804-123del	XP_005250482.1:n.1804-124_1804-123del
XM_017012318.1:c.1726-124_1726-123del	XP_016867807.1:n.1726-124_1726-123del
NM_000441.2:c.1804-124_1804-123del MANE Select	NP_000432.1:n.1804-124_1804-123del