Canonical Allele Identifier: CA352913355
Gene: GNAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193332A>C , CM000665.2:g.50193332A>C GRCh38
NC_000003.11:g.50230765A>C , CM000665.1:g.50230765A>C GRCh37
NC_000003.10:g.50205769A>C NCBI36
NG_009831.1:g.6723A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.217A>C MANE Select ENSP00000232461.3:p.Thr73Pro
ENST00000232461.7:c.217A>C ENSP00000232461.3:p.Thr73Pro
ENST00000433068.5:c.217A>C ENSP00000387555.1:p.Thr73Pro
ENST00000440836.1:c.73A>C ENSP00000403537.1:p.Thr25Pro
NM_000172.3:c.217A>C NP_000163.2:p.Thr73Pro
NM_144499.2:c.217A>C NP_653082.1:p.Thr73Pro
XM_011533595.1:c.73A>C XP_011531897.1:p.Thr25Pro
XM_011533596.1:c.73A>C XP_011531898.1:p.Thr25Pro
XR_940416.1:n.497A>C
NM_000172.4:c.217A>C NP_000163.2:p.Thr73Pro
NM_144499.3:c.217A>C MANE Select NP_653082.1:p.Thr73Pro