Canonical Allele Identifier: CA457104332

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107303813A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663368A>T , CM000669.2:g.107663368A>T	GRCh38
NC_000007.13:g.107303813A>T , CM000669.1:g.107303813A>T	GRCh37
NC_000007.12:g.107091049A>T	NCBI36
NG_008489.1:g.7734A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.237A>T MANE Select	ENSP00000494017.1:p.Arg79=
ENST00000265715.7:c.237A>T	ENSP00000265715.3:p.Arg79=
ENST00000440056.1:c.237A>T	ENSP00000394760.1:p.Arg79=
NM_000441.1:c.237A>T	NP_000432.1:p.Arg79=
XM_005250425.1:c.237A>T	XP_005250482.1:p.Arg79=
XM_006716025.2:c.237A>T	XP_006716088.1:p.Arg79=
XM_005250425.2:c.237A>T	XP_005250482.1:p.Arg79=
XM_006716025.3:c.237A>T	XP_006716088.1:p.Arg79=
XM_017012318.1:c.237A>T	XP_016867807.1:p.Arg79=
NM_000441.2:c.237A>T MANE Select	NP_000432.1:p.Arg79=