Canonical Allele Identifier: CA1363836788

Gene: GNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193417A= , CM000665.2:g.50193417A=	GRCh38
NC_000003.11:g.50230850A= , CM000665.1:g.50230850A=	GRCh37
NC_000003.10:g.50205854A=	NCBI36
NG_009831.1:g.6808A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.291+11A= MANE Select	ENSP00000232461.3:n.291+11A=
ENST00000232461.7:c.291+11A=	ENSP00000232461.3:n.291+11A=
ENST00000433068.5:c.291+11A=	ENSP00000387555.1:n.291+11A=
ENST00000440836.1:c.147+11A=	ENSP00000403537.1:n.147+11A=
NM_000172.3:c.291+11A=	NP_000163.2:n.291+11A=
NM_144499.2:c.291+11A=	NP_653082.1:n.291+11A=
XM_011533595.1:c.147+11A=	XP_011531897.1:n.147+11A=
XM_011533596.1:c.147+11A=	XP_011531898.1:n.147+11A=
XR_940416.1:n.571+11A=
NM_000172.4:c.291+11A=	NP_000163.2:n.291+11A=
NM_144499.3:c.291+11A= MANE Select	NP_653082.1:n.291+11A=