Canonical Allele Identifier: CA1363836767

Gene: GNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193373A= , CM000665.2:g.50193373A=	GRCh38
NC_000003.11:g.50230806A= , CM000665.1:g.50230806A=	GRCh37
NC_000003.10:g.50205810A=	NCBI36
NG_009831.1:g.6764A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.258A= MANE Select	ENSP00000232461.3:p.Thr86=
ENST00000232461.7:c.258A=	ENSP00000232461.3:p.Thr86=
ENST00000433068.5:c.258A=	ENSP00000387555.1:p.Thr86=
ENST00000440836.1:c.114A=	ENSP00000403537.1:p.Thr38=
NM_000172.3:c.258A=	NP_000163.2:p.Thr86=
NM_144499.2:c.258A=	NP_653082.1:p.Thr86=
XM_011533595.1:c.114A=	XP_011531897.1:p.Thr38=
XM_011533596.1:c.114A=	XP_011531898.1:p.Thr38=
XR_940416.1:n.538A=
NM_000172.4:c.258A=	NP_000163.2:p.Thr86=
NM_144499.3:c.258A= MANE Select	NP_653082.1:p.Thr86=