Canonical Allele Identifier: CA1363836602

Gene: GNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193039A= , CM000665.2:g.50193039A=	GRCh38
NC_000003.11:g.50230472A= , CM000665.1:g.50230472A=	GRCh37
NC_000003.10:g.50205476A=	NCBI36
NG_009831.1:g.6430A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000232461.8:c.107-94A= MANE Select	ENSP00000232461.3:n.107-94A=
ENST00000232461.7:c.107-94A=	ENSP00000232461.3:n.107-94A=
ENST00000433068.5:c.107-94A=	ENSP00000387555.1:n.107-94A=
ENST00000440836.1:c.-38-94A=	ENSP00000403537.1:n.-38-94A=
ENST00000467787.1:n.287+55A=
NM_000172.3:c.107-94A=	NP_000163.2:n.107-94A=
NM_144499.2:c.107-94A=	NP_653082.1:n.107-94A=
XM_011533595.1:c.-39+55A=	XP_011531897.1:n.-39+55A=
XM_011533596.1:c.-39+55A=	XP_011531898.1:n.-39+55A=
XR_940416.1:n.386+55A=
NM_000172.4:c.107-94A=	NP_000163.2:n.107-94A=
NM_144499.3:c.107-94A= MANE Select	NP_653082.1:n.107-94A=