Canonical Allele Identifier: CA1363836759
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193357T= , CM000665.2:g.50193357T= GRCh38
NC_000003.11:g.50230790T= , CM000665.1:g.50230790T= GRCh37
NC_000003.10:g.50205794T= NCBI36
NG_009831.1:g.6748T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.242T= MANE Select ENSP00000232461.3:p.Val81=
ENST00000232461.7:c.242T= ENSP00000232461.3:p.Val81=
ENST00000433068.5:c.242T= ENSP00000387555.1:p.Val81=
ENST00000440836.1:c.98T= ENSP00000403537.1:p.Val33=
NM_000172.3:c.242T= NP_000163.2:p.Val81=
NM_144499.2:c.242T= NP_653082.1:p.Val81=
XM_011533595.1:c.98T= XP_011531897.1:p.Val33=
XM_011533596.1:c.98T= XP_011531898.1:p.Val33=
XR_940416.1:n.522T=
NM_000172.4:c.242T= NP_000163.2:p.Val81=
NM_144499.3:c.242T= MANE Select NP_653082.1:p.Val81=