Canonical Allele Identifier: CA1732758436

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701135G= , CM000669.2:g.107701135G=	GRCh38
NC_000007.13:g.107341580G= , CM000669.1:g.107341580G=	GRCh37
NC_000007.12:g.107128816G=	NCBI36
NG_008489.1:g.45501G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1742G= MANE Select	ENSP00000494017.1:p.Arg581=
ENST00000644846.1:c.453G=
ENST00000265715.7:c.1742G=	ENSP00000265715.3:p.Arg581=
ENST00000480841.5:n.591G=
ENST00000492030.2:n.91-692G=
NM_000441.1:c.1742G=	NP_000432.1:p.Arg581=
XM_005250425.1:c.1742G=	XP_005250482.1:p.Arg581=
XM_005250425.2:c.1742G=	XP_005250482.1:p.Arg581=
XM_017012318.1:c.1664G=	XP_016867807.1:p.Arg555=
NM_000441.2:c.1742G= MANE Select	NP_000432.1:p.Arg581=