Canonical Allele Identifier: CA1732753313

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696069A= , CM000669.2:g.107696069A=	GRCh38
NC_000007.13:g.107336514A= , CM000669.1:g.107336514A=	GRCh37
NC_000007.12:g.107123750A=	NCBI36
NG_008489.1:g.40435A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1544+30A= MANE Select	ENSP00000494017.1:n.1544+30A=
ENST00000644846.1:c.255+30A=
ENST00000265715.7:c.1544+30A=	ENSP00000265715.3:n.1544+30A=
ENST00000477350.5:n.391+30A=
ENST00000480841.5:n.393+30A=
NM_000441.1:c.1544+30A=	NP_000432.1:n.1544+30A=
XM_005250425.1:c.1544+30A=	XP_005250482.1:n.1544+30A=
XM_005250425.2:c.1544+30A=	XP_005250482.1:n.1544+30A=
XM_017012318.1:c.1466+30A=	XP_016867807.1:n.1466+30A=
NM_000441.2:c.1544+30A= MANE Select	NP_000432.1:n.1544+30A=