Canonical Allele Identifier: CA1732753677

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696395C= , CM000669.2:g.107696395C=	GRCh38
NC_000007.13:g.107336840C= , CM000669.1:g.107336840C=	GRCh37
NC_000007.12:g.107124076C=	NCBI36
NG_008489.1:g.40761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1544+356C= MANE Select	ENSP00000494017.1:n.1544+356C=
ENST00000644846.1:c.255+356C=
ENST00000265715.7:c.1544+356C=	ENSP00000265715.3:n.1544+356C=
ENST00000477350.5:n.391+356C=
ENST00000480841.5:n.393+356C=
NM_000441.1:c.1544+356C=	NP_000432.1:n.1544+356C=
XM_005250425.1:c.1544+356C=	XP_005250482.1:n.1544+356C=
XM_005250425.2:c.1544+356C=	XP_005250482.1:n.1544+356C=
XM_017012318.1:c.1466+356C=	XP_016867807.1:n.1466+356C=
NM_000441.2:c.1544+356C= MANE Select	NP_000432.1:n.1544+356C=