Canonical Allele Identifier: CA352912016

Gene: GNAT1

Linked Data

• MyVariant Identifiers: chr3:g.50230586A>C (hg19) ; chr3:g.50193153A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193153A>C , CM000665.2:g.50193153A>C	GRCh38
NC_000003.11:g.50230586A>C , CM000665.1:g.50230586A>C	GRCh37
NC_000003.10:g.50205590A>C	NCBI36
NG_009831.1:g.6544A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000232461.8:c.127A>C MANE Select	ENSP00000232461.3:p.Ser43Arg
ENST00000232461.7:c.127A>C	ENSP00000232461.3:p.Ser43Arg
ENST00000433068.5:c.127A>C	ENSP00000387555.1:p.Ser43Arg
ENST00000440836.1:c.-18A>C	ENSP00000403537.1:n.-18A>C
ENST00000467787.1:n.308A>C
NM_000172.3:c.127A>C	NP_000163.2:p.Ser43Arg
NM_144499.2:c.127A>C	NP_653082.1:p.Ser43Arg
XM_011533595.1:c.-18A>C	XP_011531897.1:n.-18A>C
XM_011533596.1:c.-18A>C	XP_011531898.1:n.-18A>C
XR_940416.1:n.407A>C
NM_000172.4:c.127A>C	NP_000163.2:p.Ser43Arg
NM_144499.3:c.127A>C MANE Select	NP_653082.1:p.Ser43Arg