Canonical Allele Identifier: CA352913391

Gene: GNAT1

Linked Data

• MyVariant Identifiers: chr3:g.50230766C>G (hg19) ; chr3:g.50193333C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193333C>G , CM000665.2:g.50193333C>G	GRCh38
NC_000003.11:g.50230766C>G , CM000665.1:g.50230766C>G	GRCh37
NC_000003.10:g.50205770C>G	NCBI36
NG_009831.1:g.6724C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.218C>G MANE Select	ENSP00000232461.3:p.Thr73Arg
ENST00000232461.7:c.218C>G	ENSP00000232461.3:p.Thr73Arg
ENST00000433068.5:c.218C>G	ENSP00000387555.1:p.Thr73Arg
ENST00000440836.1:c.74C>G	ENSP00000403537.1:p.Thr25Arg
NM_000172.3:c.218C>G	NP_000163.2:p.Thr73Arg
NM_144499.2:c.218C>G	NP_653082.1:p.Thr73Arg
XM_011533595.1:c.74C>G	XP_011531897.1:p.Thr25Arg
XM_011533596.1:c.74C>G	XP_011531898.1:p.Thr25Arg
XR_940416.1:n.498C>G
NM_000172.4:c.218C>G	NP_000163.2:p.Thr73Arg
NM_144499.3:c.218C>G MANE Select	NP_653082.1:p.Thr73Arg