Canonical Allele Identifier: CA457093685

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107334913A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694468A>G , CM000669.2:g.107694468A>G	GRCh38
NC_000007.13:g.107334913A>G , CM000669.1:g.107334913A>G	GRCh37
NC_000007.12:g.107122149A>G	NCBI36
NG_008489.1:g.38834A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1329A>G MANE Select	ENSP00000494017.1:p.Glu443=
ENST00000644846.1:c.40A>G
ENST00000265715.7:c.1329A>G	ENSP00000265715.3:p.Glu443=
ENST00000460748.1:n.432A>G
ENST00000477350.5:n.189-153A>G
ENST00000480841.5:n.178A>G
ENST00000497446.5:n.344A>G
NM_000441.1:c.1329A>G	NP_000432.1:p.Glu443=
XM_005250425.1:c.1329A>G	XP_005250482.1:p.Glu443=
XM_005250425.2:c.1329A>G	XP_005250482.1:p.Glu443=
XM_017012318.1:c.1264-153A>G	XP_016867807.1:n.1264-153A>G
NM_000441.2:c.1329A>G MANE Select	NP_000432.1:p.Glu443=