Canonical Allele Identifier: CA2678789551

Gene: GNMT

Linked Data

• gnomAD v4: 6-42960981-C-CAGGCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960982_42960987dup , CM000668.2:g.42960982_42960987dup	GRCh38
NC_000006.11:g.42928720_42928725dup , CM000668.1:g.42928720_42928725dup	GRCh37
NC_000006.10:g.43036698_43036703dup	NCBI36
NG_008396.1:g.5221_5226dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+9_206+14dup MANE Select	ENSP00000361894.3:n.206+9_206+14dup
ENST00000372808.3:c.206+9_206+14dup	ENSP00000361894.3:n.206+9_206+14dup
NM_018960.4:c.206+9_206+14dup	NP_061833.1:n.206+9_206+14dup
XM_011514493.1:c.-13-1230_-13-1225dup	XP_011512795.1:n.-13-1230_-13-1225dup
XM_011514494.1:c.-13-1230_-13-1225dup	XP_011512796.1:n.-13-1230_-13-1225dup
NM_001318856.1:c.9-1230_9-1225dup	NP_001305785.1:n.9-1230_9-1225dup
NM_001318857.1:c.152-1780_152-1775dup	NP_001305786.1:n.152-1780_152-1775dup
NM_001318858.1:c.152-1780_152-1775dup	NP_001305787.1:n.152-1780_152-1775dup
NM_001318865.1:c.206+9_206+14dup	NP_001305794.1:n.206+9_206+14dup
NM_018960.5:c.206+9_206+14dup	NP_061833.1:n.206+9_206+14dup
NR_134890.1:n.690-1780_690-1775dup
NR_134891.1:n.593-1780_593-1775dup
NR_134892.1:n.593-1230_593-1225dup
NR_134899.1:n.220+9_220+14dup
NM_018960.6:c.206+9_206+14dup MANE Select	NP_061833.1:n.206+9_206+14dup
NM_001318856.2:c.9-1230_9-1225dup	NP_001305785.1:n.9-1230_9-1225dup
NM_001318857.2:c.152-1780_152-1775dup	NP_001305786.1:n.152-1780_152-1775dup
NM_001318858.2:c.152-1780_152-1775dup	NP_001305787.1:n.152-1780_152-1775dup
NM_001318865.2:c.206+9_206+14dup	NP_001305794.1:n.206+9_206+14dup
NR_134890.2:n.340-1780_340-1775dup
NR_134891.2:n.243-1780_243-1775dup
NR_134892.2:n.243-1230_243-1225dup
NR_134899.2:n.220+9_220+14dup