Canonical Allele Identifier: CA1363836801

Gene: GNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193435T= , CM000665.2:g.50193435T=	GRCh38
NC_000003.11:g.50230868T= , CM000665.1:g.50230868T=	GRCh37
NC_000003.10:g.50205872T=	NCBI36
NG_009831.1:g.6826T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.291+29T= MANE Select	ENSP00000232461.3:n.291+29T=
ENST00000232461.7:c.291+29T=	ENSP00000232461.3:n.291+29T=
ENST00000433068.5:c.291+29T=	ENSP00000387555.1:n.291+29T=
ENST00000440836.1:c.147+29T=	ENSP00000403537.1:n.147+29T=
NM_000172.3:c.291+29T=	NP_000163.2:n.291+29T=
NM_144499.2:c.291+29T=	NP_653082.1:n.291+29T=
XM_011533595.1:c.147+29T=	XP_011531897.1:n.147+29T=
XM_011533596.1:c.147+29T=	XP_011531898.1:n.147+29T=
XR_940416.1:n.571+29T=
NM_000172.4:c.291+29T=	NP_000163.2:n.291+29T=
NM_144499.3:c.291+29T= MANE Select	NP_653082.1:n.291+29T=