Canonical Allele Identifier: CA419369800

Gene: GNAT2 GNAI3

Linked Data

• MyVariant Identifiers: chr1:g.110152662C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109610040C>A , CM000663.2:g.109610040C>A	GRCh38
NC_000001.10:g.110152662C>A , CM000663.1:g.110152662C>A	GRCh37
NC_000001.9:g.109954185C>A	NCBI36
NG_009099.1:g.8044G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000351050.8:c.303G>T (GNAT2)	ENSP00000251337.3:p.Ala101=
ENST00000679935.1:c.303G>T (GNAT2) MANE Select	ENSP00000505083.1:p.Ala101=
ENST00000351050.7:c.303G>T (GNAT2)	ENSP00000251337.3:p.Ala101=
ENST00000369851.5:c.*17718C>A (GNAI3)	ENSP00000358867.4:n.*17718C>A
ENST00000622865.1:c.303G>T (GNAT2)	ENSP00000482596.1:p.Ala101=
NM_005272.3:c.303G>T (GNAT2)	NP_005263.1:p.Ala101=
XM_011541264.1:c.303G>T (GNAT2)	XP_011539566.1:p.Ala101=
XM_011541265.1:c.303G>T (GNAT2)	XP_011539567.1:p.Ala101=
XM_011541266.1:c.303G>T (GNAT2)	XP_011539568.1:p.Ala101=
XM_011541264.2:c.303G>T (GNAT2)	XP_011539566.1:p.Ala101=
NM_001377295.1:c.303G>T (GNAT2)	NP_001364224.1:p.Ala101=
NM_005272.5:c.303G>T (GNAT2)	NP_005263.1:p.Ala101=
NM_001377295.2:c.303G>T (GNAT2) MANE Select	NP_001364224.1:p.Ala101=
NM_001379232.1:c.303G>T (GNAT2)	NP_001366161.1:p.Ala101=