Canonical Allele Identifier: CA824892535

Gene: GNMT

Linked Data

• dbSNP Id: rs1436443786
• gnomAD v3: 6-42961177-C-CG
• gnomAD v4: 6-42961177-C-CG
• MyVariant Identifiers: chr6:g.42928915_42928916insG (hg19) ; chr6:g.42961177_42961178insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961179dup , CM000668.2:g.42961179dup	GRCh38
NC_000006.11:g.42928917dup , CM000668.1:g.42928917dup	GRCh37
NC_000006.10:g.43036895dup	NCBI36
NG_008396.1:g.5418dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+206dup MANE Select	ENSP00000361894.3:n.206+206dup
ENST00000372808.3:c.206+206dup	ENSP00000361894.3:n.206+206dup
NM_018960.4:c.206+206dup	NP_061833.1:n.206+206dup
XM_011514493.1:c.-13-1033dup	XP_011512795.1:n.-13-1033dup
XM_011514494.1:c.-13-1033dup	XP_011512796.1:n.-13-1033dup
NM_001318856.1:c.9-1033dup	NP_001305785.1:n.9-1033dup
NM_001318857.1:c.152-1583dup	NP_001305786.1:n.152-1583dup
NM_001318858.1:c.152-1583dup	NP_001305787.1:n.152-1583dup
NM_001318865.1:c.206+206dup	NP_001305794.1:n.206+206dup
NM_018960.5:c.206+206dup	NP_061833.1:n.206+206dup
NR_134890.1:n.690-1583dup
NR_134891.1:n.593-1583dup
NR_134892.1:n.593-1033dup
NR_134899.1:n.220+206dup
NM_018960.6:c.206+206dup MANE Select	NP_061833.1:n.206+206dup
NM_001318856.2:c.9-1033dup	NP_001305785.1:n.9-1033dup
NM_001318857.2:c.152-1583dup	NP_001305786.1:n.152-1583dup
NM_001318858.2:c.152-1583dup	NP_001305787.1:n.152-1583dup
NM_001318865.2:c.206+206dup	NP_001305794.1:n.206+206dup
NR_134890.2:n.340-1583dup
NR_134891.2:n.243-1583dup
NR_134892.2:n.243-1033dup
NR_134899.2:n.220+206dup