Canonical Allele Identifier: CA433860432

Gene: GNAT1

Linked Data

• MyVariant Identifiers: chr3:g.50230743T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193310T>C , CM000665.2:g.50193310T>C	GRCh38
NC_000003.11:g.50230743T>C , CM000665.1:g.50230743T>C	GRCh37
NC_000003.10:g.50205747T>C	NCBI36
NG_009831.1:g.6701T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.195T>C MANE Select	ENSP00000232461.3:p.Phe65=
ENST00000232461.7:c.195T>C	ENSP00000232461.3:p.Phe65=
ENST00000433068.5:c.195T>C	ENSP00000387555.1:p.Phe65=
ENST00000440836.1:c.51T>C	ENSP00000403537.1:p.Phe17=
NM_000172.3:c.195T>C	NP_000163.2:p.Phe65=
NM_144499.2:c.195T>C	NP_653082.1:p.Phe65=
XM_011533595.1:c.51T>C	XP_011531897.1:p.Phe17=
XM_011533596.1:c.51T>C	XP_011531898.1:p.Phe17=
XR_940416.1:n.475T>C
NM_000172.4:c.195T>C	NP_000163.2:p.Phe65=
NM_144499.3:c.195T>C MANE Select	NP_653082.1:p.Phe65=