Canonical Allele Identifier: CA1732757162

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107717422T= , CM000669.2:g.107717422T=	GRCh38
NC_000007.13:g.107357867T= , CM000669.1:g.107357867T=	GRCh37
NC_000007.12:g.107145103T=	NCBI36
NG_008489.1:g.61788T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.*1976T= MANE Select	ENSP00000494017.1:n.*1976T=
ENST00000265715.7:c.*1976T=	ENSP00000265715.3:n.*1976T=
NM_000441.1:c.*1976T=	NP_000432.1:n.*1976T=
NM_000441.2:c.*1976T= MANE Select	NP_000432.1:n.*1976T=