Canonical Allele Identifier: CA352911962

Gene: GNAT1

Linked Data

• dbSNP Id: rs1699439597
• MyVariant Identifiers: chr3:g.50230581G>C (hg19) ; chr3:g.50193148G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193148G>C , CM000665.2:g.50193148G>C	GRCh38
NC_000003.11:g.50230581G>C , CM000665.1:g.50230581G>C	GRCh37
NC_000003.10:g.50205585G>C	NCBI36
NG_009831.1:g.6539G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000232461.8:c.122G>C MANE Select	ENSP00000232461.3:p.Gly41Ala
ENST00000232461.7:c.122G>C	ENSP00000232461.3:p.Gly41Ala
ENST00000433068.5:c.122G>C	ENSP00000387555.1:p.Gly41Ala
ENST00000440836.1:c.-23G>C	ENSP00000403537.1:n.-23G>C
ENST00000467787.1:n.303G>C
NM_000172.3:c.122G>C	NP_000163.2:p.Gly41Ala
NM_144499.2:c.122G>C	NP_653082.1:p.Gly41Ala
XM_011533595.1:c.-23G>C	XP_011531897.1:n.-23G>C
XM_011533596.1:c.-23G>C	XP_011531898.1:n.-23G>C
XR_940416.1:n.402G>C
NM_000172.4:c.122G>C	NP_000163.2:p.Gly41Ala
NM_144499.3:c.122G>C MANE Select	NP_653082.1:p.Gly41Ala