Canonical Allele Identifier: CA1624303922

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961245_42961246delinsGC , CM000668.2:g.42961245_42961246delinsGC	GRCh38
NC_000006.11:g.42928983_42928984delinsGC , CM000668.1:g.42928983_42928984delinsGC	GRCh37
NC_000006.10:g.43036961_43036962delinsGC	NCBI36
NG_008396.1:g.5484_5485delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+272_206+273delinsGC MANE Select	ENSP00000361894.3:n.206+272_206+273delinsGC
ENST00000372808.3:c.206+272_206+273delinsGC	ENSP00000361894.3:n.206+272_206+273delinsGC
NM_018960.4:c.206+272_206+273delinsGC	NP_061833.1:n.206+272_206+273delinsGC
XM_011514493.1:c.-13-967_-13-966delinsGC	XP_011512795.1:n.-13-967_-13-966delinsGC
XM_011514494.1:c.-13-967_-13-966delinsGC	XP_011512796.1:n.-13-967_-13-966delinsGC
NM_001318856.1:c.9-967_9-966delinsGC	NP_001305785.1:n.9-967_9-966delinsGC
NM_001318857.1:c.152-1517_152-1516delinsGC	NP_001305786.1:n.152-1517_152-1516delinsGC
NM_001318858.1:c.152-1517_152-1516delinsGC	NP_001305787.1:n.152-1517_152-1516delinsGC
NM_001318865.1:c.206+272_206+273delinsGC	NP_001305794.1:n.206+272_206+273delinsGC
NM_018960.5:c.206+272_206+273delinsGC	NP_061833.1:n.206+272_206+273delinsGC
NR_134890.1:n.690-1517_690-1516delinsGC
NR_134891.1:n.593-1517_593-1516delinsGC
NR_134892.1:n.593-967_593-966delinsGC
NR_134899.1:n.220+272_220+273delinsGC
NM_018960.6:c.206+272_206+273delinsGC MANE Select	NP_061833.1:n.206+272_206+273delinsGC
NM_001318856.2:c.9-967_9-966delinsGC	NP_001305785.1:n.9-967_9-966delinsGC
NM_001318857.2:c.152-1517_152-1516delinsGC	NP_001305786.1:n.152-1517_152-1516delinsGC
NM_001318858.2:c.152-1517_152-1516delinsGC	NP_001305787.1:n.152-1517_152-1516delinsGC
NM_001318865.2:c.206+272_206+273delinsGC	NP_001305794.1:n.206+272_206+273delinsGC
NR_134890.2:n.340-1517_340-1516delinsGC
NR_134891.2:n.243-1517_243-1516delinsGC
NR_134892.2:n.243-967_243-966delinsGC
NR_134899.2:n.220+272_220+273delinsGC