Canonical Allele Identifier: CA1624303887

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961210_42961212delinsCTG , CM000668.2:g.42961210_42961212delinsCTG	GRCh38
NC_000006.11:g.42928948_42928950delinsCTG , CM000668.1:g.42928948_42928950delinsCTG	GRCh37
NC_000006.10:g.43036926_43036928delinsCTG	NCBI36
NG_008396.1:g.5449_5451delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+237_206+239delinsCTG MANE Select	ENSP00000361894.3:n.206+237_206+239delinsCTG
ENST00000372808.3:c.206+237_206+239delinsCTG	ENSP00000361894.3:n.206+237_206+239delinsCTG
NM_018960.4:c.206+237_206+239delinsCTG	NP_061833.1:n.206+237_206+239delinsCTG
XM_011514493.1:c.-13-1002_-13-1000delinsCTG	XP_011512795.1:n.-13-1002_-13-1000delinsCTG
XM_011514494.1:c.-13-1002_-13-1000delinsCTG	XP_011512796.1:n.-13-1002_-13-1000delinsCTG
NM_001318856.1:c.9-1002_9-1000delinsCTG	NP_001305785.1:n.9-1002_9-1000delinsCTG
NM_001318857.1:c.152-1552_152-1550delinsCTG	NP_001305786.1:n.152-1552_152-1550delinsCTG
NM_001318858.1:c.152-1552_152-1550delinsCTG	NP_001305787.1:n.152-1552_152-1550delinsCTG
NM_001318865.1:c.206+237_206+239delinsCTG	NP_001305794.1:n.206+237_206+239delinsCTG
NM_018960.5:c.206+237_206+239delinsCTG	NP_061833.1:n.206+237_206+239delinsCTG
NR_134890.1:n.690-1552_690-1550delinsCTG
NR_134891.1:n.593-1552_593-1550delinsCTG
NR_134892.1:n.593-1002_593-1000delinsCTG
NR_134899.1:n.220+237_220+239delinsCTG
NM_018960.6:c.206+237_206+239delinsCTG MANE Select	NP_061833.1:n.206+237_206+239delinsCTG
NM_001318856.2:c.9-1002_9-1000delinsCTG	NP_001305785.1:n.9-1002_9-1000delinsCTG
NM_001318857.2:c.152-1552_152-1550delinsCTG	NP_001305786.1:n.152-1552_152-1550delinsCTG
NM_001318858.2:c.152-1552_152-1550delinsCTG	NP_001305787.1:n.152-1552_152-1550delinsCTG
NM_001318865.2:c.206+237_206+239delinsCTG	NP_001305794.1:n.206+237_206+239delinsCTG
NR_134890.2:n.340-1552_340-1550delinsCTG
NR_134891.2:n.243-1552_243-1550delinsCTG
NR_134892.2:n.243-1002_243-1000delinsCTG
NR_134899.2:n.220+237_220+239delinsCTG