Canonical Allele Identifier: CA1363836784
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193407G= , CM000665.2:g.50193407G= GRCh38
NC_000003.11:g.50230840G= , CM000665.1:g.50230840G= GRCh37
NC_000003.10:g.50205844G= NCBI36
NG_009831.1:g.6798G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.291+1G= MANE Select ENSP00000232461.3:n.291+1G=
ENST00000232461.7:c.291+1G= ENSP00000232461.3:n.291+1G=
ENST00000433068.5:c.291+1G= ENSP00000387555.1:n.291+1G=
ENST00000440836.1:c.147+1G= ENSP00000403537.1:n.147+1G=
NM_000172.3:c.291+1G= NP_000163.2:n.291+1G=
NM_144499.2:c.291+1G= NP_653082.1:n.291+1G=
XM_011533595.1:c.147+1G= XP_011531897.1:n.147+1G=
XM_011533596.1:c.147+1G= XP_011531898.1:n.147+1G=
XR_940416.1:n.571+1G=
NM_000172.4:c.291+1G= NP_000163.2:n.291+1G=
NM_144499.3:c.291+1G= MANE Select NP_653082.1:n.291+1G=