Canonical Allele Identifier: CA457096443

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107336464T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696019T>G , CM000669.2:g.107696019T>G	GRCh38
NC_000007.13:g.107336464T>G , CM000669.1:g.107336464T>G	GRCh37
NC_000007.12:g.107123700T>G	NCBI36
NG_008489.1:g.40385T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1524T>G MANE Select	ENSP00000494017.1:p.Thr508=
ENST00000644846.1:c.235T>G
ENST00000265715.7:c.1524T>G	ENSP00000265715.3:p.Thr508=
ENST00000477350.5:n.371T>G
ENST00000480841.5:n.373T>G
ENST00000497446.5:n.539T>G
NM_000441.1:c.1524T>G	NP_000432.1:p.Thr508=
XM_005250425.1:c.1524T>G	XP_005250482.1:p.Thr508=
XM_005250425.2:c.1524T>G	XP_005250482.1:p.Thr508=
XM_017012318.1:c.1446T>G	XP_016867807.1:p.Thr482=
NM_000441.2:c.1524T>G MANE Select	NP_000432.1:p.Thr508=