Canonical Allele Identifier: CA1732758200

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791870704
• gnomAD v4: 7-107701038-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701039del , CM000669.2:g.107701039del	GRCh38
NC_000007.13:g.107341484del , CM000669.1:g.107341484del	GRCh37
NC_000007.12:g.107128720del	NCBI36
NG_008489.1:g.45405del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1708-62del MANE Select	ENSP00000494017.1:n.1708-62del
ENST00000644846.1:c.419-62del
ENST00000265715.7:c.1708-62del	ENSP00000265715.3:n.1708-62del
ENST00000480841.5:n.557-62del
ENST00000492030.2:n.91-788del
NM_000441.1:c.1708-62del	NP_000432.1:n.1708-62del
XM_005250425.1:c.1708-62del	XP_005250482.1:n.1708-62del
XM_005250425.2:c.1708-62del	XP_005250482.1:n.1708-62del
XM_017012318.1:c.1630-62del	XP_016867807.1:n.1630-62del
NM_000441.2:c.1708-62del MANE Select	NP_000432.1:n.1708-62del