Canonical Allele Identifier: CA1732751295

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694334A= , CM000669.2:g.107694334A=	GRCh38
NC_000007.13:g.107334779A= , CM000669.1:g.107334779A=	GRCh37
NC_000007.12:g.107122015A=	NCBI36
NG_008489.1:g.38700A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1264-69A= MANE Select	ENSP00000494017.1:n.1264-69A=
ENST00000265715.7:c.1264-69A=	ENSP00000265715.3:n.1264-69A=
ENST00000460748.1:n.367-69A=
ENST00000477350.5:n.189-287A=
ENST00000480841.5:n.113-69A=
ENST00000497446.5:n.279-69A=
NM_000441.1:c.1264-69A=	NP_000432.1:n.1264-69A=
XM_005250425.1:c.1264-69A=	XP_005250482.1:n.1264-69A=
XM_006716025.2:c.*774A=	XP_006716088.1:n.*774A=
XM_005250425.2:c.1264-69A=	XP_005250482.1:n.1264-69A=
XM_006716025.3:c.*774A=	XP_006716088.1:n.*774A=
XM_017012318.1:c.1264-287A=	XP_016867807.1:n.1264-287A=
NM_000441.2:c.1264-69A= MANE Select	NP_000432.1:n.1264-69A=