Canonical Allele Identifier: CA1363836753
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193346C= , CM000665.2:g.50193346C= GRCh38
NC_000003.11:g.50230779C= , CM000665.1:g.50230779C= GRCh37
NC_000003.10:g.50205783C= NCBI36
NG_009831.1:g.6737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.231C= MANE Select ENSP00000232461.3:p.Ile77=
ENST00000232461.7:c.231C= ENSP00000232461.3:p.Ile77=
ENST00000433068.5:c.231C= ENSP00000387555.1:p.Ile77=
ENST00000440836.1:c.87C= ENSP00000403537.1:p.Ile29=
NM_000172.3:c.231C= NP_000163.2:p.Ile77=
NM_144499.2:c.231C= NP_653082.1:p.Ile77=
XM_011533595.1:c.87C= XP_011531897.1:p.Ile29=
XM_011533596.1:c.87C= XP_011531898.1:p.Ile29=
XR_940416.1:n.511C=
NM_000172.4:c.231C= NP_000163.2:p.Ile77=
NM_144499.3:c.231C= MANE Select NP_653082.1:p.Ile77=