Canonical Allele Identifier: CA433860536

Gene: GNAT1

Linked Data

• MyVariant Identifiers: chr3:g.50230791A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193358A>C , CM000665.2:g.50193358A>C	GRCh38
NC_000003.11:g.50230791A>C , CM000665.1:g.50230791A>C	GRCh37
NC_000003.10:g.50205795A>C	NCBI36
NG_009831.1:g.6749A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.243A>C MANE Select	ENSP00000232461.3:p.Val81=
ENST00000232461.7:c.243A>C	ENSP00000232461.3:p.Val81=
ENST00000433068.5:c.243A>C	ENSP00000387555.1:p.Val81=
ENST00000440836.1:c.99A>C	ENSP00000403537.1:p.Val33=
NM_000172.3:c.243A>C	NP_000163.2:p.Val81=
NM_144499.2:c.243A>C	NP_653082.1:p.Val81=
XM_011533595.1:c.99A>C	XP_011531897.1:p.Val33=
XM_011533596.1:c.99A>C	XP_011531898.1:p.Val33=
XR_940416.1:n.523A>C
NM_000172.4:c.243A>C	NP_000163.2:p.Val81=
NM_144499.3:c.243A>C MANE Select	NP_653082.1:p.Val81=