Canonical Allele Identifier: CA457096268

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107336443C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695998C>G , CM000669.2:g.107695998C>G	GRCh38
NC_000007.13:g.107336443C>G , CM000669.1:g.107336443C>G	GRCh37
NC_000007.12:g.107123679C>G	NCBI36
NG_008489.1:g.40364C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1503C>G MANE Select	ENSP00000494017.1:p.Gly501=
ENST00000644846.1:c.214C>G
ENST00000265715.7:c.1503C>G	ENSP00000265715.3:p.Gly501=
ENST00000477350.5:n.350C>G
ENST00000480841.5:n.352C>G
ENST00000497446.5:n.518C>G
NM_000441.1:c.1503C>G	NP_000432.1:p.Gly501=
XM_005250425.1:c.1503C>G	XP_005250482.1:p.Gly501=
XM_005250425.2:c.1503C>G	XP_005250482.1:p.Gly501=
XM_017012318.1:c.1425C>G	XP_016867807.1:p.Gly475=
NM_000441.2:c.1503C>G MANE Select	NP_000432.1:p.Gly501=