Canonical Allele Identifier: CA1624303317
Gene: GNMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42960823C= , CM000668.2:g.42960823C= GRCh38
NC_000006.11:g.42928561C= , CM000668.1:g.42928561C= GRCh37
NC_000006.10:g.43036539C= NCBI36
NG_008396.1:g.5062C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372808.4:c.56C= MANE Select ENSP00000361894.3:p.Pro19=
ENST00000372808.3:c.56C= ENSP00000361894.3:p.Pro19=
NM_018960.4:c.56C= NP_061833.1:p.Pro19=
XM_011514493.1:c.-13-1389C= XP_011512795.1:n.-13-1389C=
XM_011514494.1:c.-13-1389C= XP_011512796.1:n.-13-1389C=
NM_001318856.1:c.9-1389C= NP_001305785.1:n.9-1389C=
NM_001318857.1:c.152-1939C= NP_001305786.1:n.152-1939C=
NM_001318858.1:c.152-1939C= NP_001305787.1:n.152-1939C=
NM_001318865.1:c.56C= NP_001305794.1:p.Pro19=
NM_018960.5:c.56C= NP_061833.1:p.Pro19=
NR_134890.1:n.690-1939C=
NR_134891.1:n.593-1939C=
NR_134892.1:n.593-1389C=
NR_134899.1:n.70C=
NM_018960.6:c.56C= MANE Select NP_061833.1:p.Pro19=
NM_001318856.2:c.9-1389C= NP_001305785.1:n.9-1389C=
NM_001318857.2:c.152-1939C= NP_001305786.1:n.152-1939C=
NM_001318858.2:c.152-1939C= NP_001305787.1:n.152-1939C=
NM_001318865.2:c.56C= NP_001305794.1:p.Pro19=
NR_134890.2:n.340-1939C=
NR_134891.2:n.243-1939C=
NR_134892.2:n.243-1389C=
NR_134899.2:n.70C=