Canonical Allele Identifier: CA368841330

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107336453G>T (hg19) ; chr7:g.107696008G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696008G>T , CM000669.2:g.107696008G>T	GRCh38
NC_000007.13:g.107336453G>T , CM000669.1:g.107336453G>T	GRCh37
NC_000007.12:g.107123689G>T	NCBI36
NG_008489.1:g.40374G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1513G>T MANE Select	ENSP00000494017.1:p.Gly505Ter
ENST00000644846.1:c.224G>T
ENST00000265715.7:c.1513G>T	ENSP00000265715.3:p.Gly505Ter
ENST00000477350.5:n.360G>T
ENST00000480841.5:n.362G>T
ENST00000497446.5:n.528G>T
NM_000441.1:c.1513G>T	NP_000432.1:p.Gly505Ter
XM_005250425.1:c.1513G>T	XP_005250482.1:p.Gly505Ter
XM_005250425.2:c.1513G>T	XP_005250482.1:p.Gly505Ter
XM_017012318.1:c.1435G>T	XP_016867807.1:p.Gly479Ter
NM_000441.2:c.1513G>T MANE Select	NP_000432.1:p.Gly505Ter