Canonical Allele Identifier: CA1732759079

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701815T= , CM000669.2:g.107701815T=	GRCh38
NC_000007.13:g.107342260T= , CM000669.1:g.107342260T=	GRCh37
NC_000007.12:g.107129496T=	NCBI36
NG_008489.1:g.46181T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1804-12T= MANE Select	ENSP00000494017.1:n.1804-12T=
ENST00000644846.1:c.515-12T=
ENST00000265715.7:c.1804-12T=	ENSP00000265715.3:n.1804-12T=
ENST00000480841.5:n.653-12T=
ENST00000492030.2:n.91-12T=
NM_000441.1:c.1804-12T=	NP_000432.1:n.1804-12T=
XM_005250425.1:c.1804-12T=	XP_005250482.1:n.1804-12T=
XM_005250425.2:c.1804-12T=	XP_005250482.1:n.1804-12T=
XM_017012318.1:c.1726-12T=	XP_016867807.1:n.1726-12T=
NM_000441.2:c.1804-12T= MANE Select	NP_000432.1:n.1804-12T=