Canonical Allele Identifier: CA1363836668
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193150A= , CM000665.2:g.50193150A= GRCh38
NC_000003.11:g.50230583A= , CM000665.1:g.50230583A= GRCh37
NC_000003.10:g.50205587A= NCBI36
NG_009831.1:g.6541A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.124A= MANE Select ENSP00000232461.3:p.Lys42=
ENST00000232461.7:c.124A= ENSP00000232461.3:p.Lys42=
ENST00000433068.5:c.124A= ENSP00000387555.1:p.Lys42=
ENST00000440836.1:c.-21A= ENSP00000403537.1:n.-21A=
ENST00000467787.1:n.305A=
NM_000172.3:c.124A= NP_000163.2:p.Lys42=
NM_144499.2:c.124A= NP_653082.1:p.Lys42=
XM_011533595.1:c.-21A= XP_011531897.1:n.-21A=
XM_011533596.1:c.-21A= XP_011531898.1:n.-21A=
XR_940416.1:n.404A=
NM_000172.4:c.124A= NP_000163.2:p.Lys42=
NM_144499.3:c.124A= MANE Select NP_653082.1:p.Lys42=