Canonical Allele Identifier: CA1363836613
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193058T= , CM000665.2:g.50193058T= GRCh38
NC_000003.11:g.50230491T= , CM000665.1:g.50230491T= GRCh37
NC_000003.10:g.50205495T= NCBI36
NG_009831.1:g.6449T=

Transcript Alleles

HGVS Amino-acid change
ENST00000232461.8:c.107-75T= MANE Select ENSP00000232461.3:n.107-75T=
ENST00000232461.7:c.107-75T= ENSP00000232461.3:n.107-75T=
ENST00000433068.5:c.107-75T= ENSP00000387555.1:n.107-75T=
ENST00000440836.1:c.-38-75T= ENSP00000403537.1:n.-38-75T=
ENST00000467787.1:n.288-75T=
NM_000172.3:c.107-75T= NP_000163.2:n.107-75T=
NM_144499.2:c.107-75T= NP_653082.1:n.107-75T=
XM_011533595.1:c.-38-75T= XP_011531897.1:n.-38-75T=
XM_011533596.1:c.-38-75T= XP_011531898.1:n.-38-75T=
XR_940416.1:n.387-75T=
NM_000172.4:c.107-75T= NP_000163.2:n.107-75T=
NM_144499.3:c.107-75T= MANE Select NP_653082.1:n.107-75T=