Canonical Allele Identifier: CA1363836669
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193152G= , CM000665.2:g.50193152G= GRCh38
NC_000003.11:g.50230585G= , CM000665.1:g.50230585G= GRCh37
NC_000003.10:g.50205589G= NCBI36
NG_009831.1:g.6543G=

Transcript Alleles

HGVS Amino-acid change
ENST00000232461.8:c.126G= MANE Select ENSP00000232461.3:p.Lys42=
ENST00000232461.7:c.126G= ENSP00000232461.3:p.Lys42=
ENST00000433068.5:c.126G= ENSP00000387555.1:p.Lys42=
ENST00000440836.1:c.-19G= ENSP00000403537.1:n.-19G=
ENST00000467787.1:n.307G=
NM_000172.3:c.126G= NP_000163.2:p.Lys42=
NM_144499.2:c.126G= NP_653082.1:p.Lys42=
XM_011533595.1:c.-19G= XP_011531897.1:n.-19G=
XM_011533596.1:c.-19G= XP_011531898.1:n.-19G=
XR_940416.1:n.406G=
NM_000172.4:c.126G= NP_000163.2:p.Lys42=
NM_144499.3:c.126G= MANE Select NP_653082.1:p.Lys42=