Canonical Allele Identifier: CA352913039
Gene: GNAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193309T>G , CM000665.2:g.50193309T>G GRCh38
NC_000003.11:g.50230742T>G , CM000665.1:g.50230742T>G GRCh37
NC_000003.10:g.50205746T>G NCBI36
NG_009831.1:g.6700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.194T>G MANE Select ENSP00000232461.3:p.Phe65Cys
ENST00000232461.7:c.194T>G ENSP00000232461.3:p.Phe65Cys
ENST00000433068.5:c.194T>G ENSP00000387555.1:p.Phe65Cys
ENST00000440836.1:c.50T>G ENSP00000403537.1:p.Phe17Cys
NM_000172.3:c.194T>G NP_000163.2:p.Phe65Cys
NM_144499.2:c.194T>G NP_653082.1:p.Phe65Cys
XM_011533595.1:c.50T>G XP_011531897.1:p.Phe17Cys
XM_011533596.1:c.50T>G XP_011531898.1:p.Phe17Cys
XR_940416.1:n.474T>G
NM_000172.4:c.194T>G NP_000163.2:p.Phe65Cys
NM_144499.3:c.194T>G MANE Select NP_653082.1:p.Phe65Cys