Canonical Allele Identifier: CA341539615

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109608631T>A , CM000663.2:g.109608631T>A GRCh38
NC_000001.10:g.110151253T>A , CM000663.1:g.110151253T>A GRCh37
NC_000001.9:g.109952776T>A NCBI36
NG_009099.1:g.9453A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351050.8:c.461A>T (GNAT2) ENSP00000251337.3:p.Tyr154Phe
ENST00000679935.1:c.461A>T (GNAT2) MANE Select ENSP00000505083.1:p.Tyr154Phe
ENST00000351050.7:c.461A>T (GNAT2) ENSP00000251337.3:p.Tyr154Phe
ENST00000369851.5:c.*16309T>A (GNAI3) ENSP00000358867.4:n.*16309T>A
NM_005272.3:c.461A>T (GNAT2) NP_005263.1:p.Tyr154Phe
XM_011541264.1:c.461A>T (GNAT2) XP_011539566.1:p.Tyr154Phe
XM_011541265.1:c.461A>T (GNAT2) XP_011539567.1:p.Tyr154Phe
XM_011541266.1:c.461A>T (GNAT2) XP_011539568.1:p.Tyr154Phe
XM_011541264.2:c.461A>T (GNAT2) XP_011539566.1:p.Tyr154Phe
NM_001377295.1:c.461A>T (GNAT2) NP_001364224.1:p.Tyr154Phe
NM_005272.5:c.461A>T (GNAT2) NP_005263.1:p.Tyr154Phe
NM_001377295.2:c.461A>T (GNAT2) MANE Select NP_001364224.1:p.Tyr154Phe
NM_001379232.1:c.461A>T (GNAT2) NP_001366161.1:p.Tyr154Phe