Canonical Allele Identifier: CA352913641
Gene: GNAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1406092062
gnomAD v2: 3-50230792-C-T
gnomAD v4: 3-50193359-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193359C>T , CM000665.2:g.50193359C>T GRCh38
NC_000003.11:g.50230792C>T , CM000665.1:g.50230792C>T GRCh37
NC_000003.10:g.50205796C>T NCBI36
NG_009831.1:g.6750C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.244C>T MANE Select ENSP00000232461.3:p.Arg82Cys
ENST00000232461.7:c.244C>T ENSP00000232461.3:p.Arg82Cys
ENST00000433068.5:c.244C>T ENSP00000387555.1:p.Arg82Cys
ENST00000440836.1:c.100C>T ENSP00000403537.1:p.Arg34Cys
NM_000172.3:c.244C>T NP_000163.2:p.Arg82Cys
NM_144499.2:c.244C>T NP_653082.1:p.Arg82Cys
XM_011533595.1:c.100C>T XP_011531897.1:p.Arg34Cys
XM_011533596.1:c.100C>T XP_011531898.1:p.Arg34Cys
XR_940416.1:n.524C>T
NM_000172.4:c.244C>T NP_000163.2:p.Arg82Cys
NM_144499.3:c.244C>T MANE Select NP_653082.1:p.Arg82Cys