Canonical Allele Identifier: CA1624303518
Gene: GNMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42960923_42960924delinsGC , CM000668.2:g.42960923_42960924delinsGC GRCh38
NC_000006.11:g.42928661_42928662delinsGC , CM000668.1:g.42928661_42928662delinsGC GRCh37
NC_000006.10:g.43036639_43036640delinsGC NCBI36
NG_008396.1:g.5162_5163delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000372808.4:c.156_157delinsGC MANE Select ENSP00000361894.3:p.Leu52=
ENST00000372808.3:c.156_157delinsGC ENSP00000361894.3:p.Leu52=
NM_018960.4:c.156_157delinsGC NP_061833.1:p.Leu52=
XM_011514493.1:c.-13-1289_-13-1288delinsGC XP_011512795.1:n.-13-1289_-13-1288delinsG...
XM_011514494.1:c.-13-1289_-13-1288delinsGC XP_011512796.1:n.-13-1289_-13-1288delinsG...
NM_001318856.1:c.9-1289_9-1288delinsGC NP_001305785.1:n.9-1289_9-1288delinsGC
NM_001318857.1:c.152-1839_152-1838delinsGC NP_001305786.1:n.152-1839_152-1838delinsG...
NM_001318858.1:c.152-1839_152-1838delinsGC NP_001305787.1:n.152-1839_152-1838delinsG...
NM_001318865.1:c.156_157delinsGC NP_001305794.1:p.Leu52=
NM_018960.5:c.156_157delinsGC NP_061833.1:p.Leu52=
NR_134890.1:n.690-1839_690-1838delinsGC
NR_134891.1:n.593-1839_593-1838delinsGC
NR_134892.1:n.593-1289_593-1288delinsGC
NR_134899.1:n.170_171delinsGC
NM_018960.6:c.156_157delinsGC MANE Select NP_061833.1:p.Leu52=
NM_001318856.2:c.9-1289_9-1288delinsGC NP_001305785.1:n.9-1289_9-1288delinsGC
NM_001318857.2:c.152-1839_152-1838delinsGC NP_001305786.1:n.152-1839_152-1838delinsG...
NM_001318858.2:c.152-1839_152-1838delinsGC NP_001305787.1:n.152-1839_152-1838delinsG...
NM_001318865.2:c.156_157delinsGC NP_001305794.1:p.Leu52=
NR_134890.2:n.340-1839_340-1838delinsGC
NR_134891.2:n.243-1839_243-1838delinsGC
NR_134892.2:n.243-1289_243-1288delinsGC
NR_134899.2:n.170_171delinsGC