Canonical Allele Identifier: CA1624303925

Gene: GNMT

Linked Data

• dbSNP Id: rs1769372569

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961246del , CM000668.2:g.42961246del	GRCh38
NC_000006.11:g.42928984del , CM000668.1:g.42928984del	GRCh37
NC_000006.10:g.43036962del	NCBI36
NG_008396.1:g.5485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+273del MANE Select	ENSP00000361894.3:n.206+273del
ENST00000372808.3:c.206+273del	ENSP00000361894.3:n.206+273del
NM_018960.4:c.206+273del	NP_061833.1:n.206+273del
XM_011514493.1:c.-13-966del	XP_011512795.1:n.-13-966del
XM_011514494.1:c.-13-966del	XP_011512796.1:n.-13-966del
NM_001318856.1:c.9-966del	NP_001305785.1:n.9-966del
NM_001318857.1:c.152-1516del	NP_001305786.1:n.152-1516del
NM_001318858.1:c.152-1516del	NP_001305787.1:n.152-1516del
NM_001318865.1:c.206+273del	NP_001305794.1:n.206+273del
NM_018960.5:c.206+273del	NP_061833.1:n.206+273del
NR_134890.1:n.690-1516del
NR_134891.1:n.593-1516del
NR_134892.1:n.593-966del
NR_134899.1:n.220+273del
NM_018960.6:c.206+273del MANE Select	NP_061833.1:n.206+273del
NM_001318856.2:c.9-966del	NP_001305785.1:n.9-966del
NM_001318857.2:c.152-1516del	NP_001305786.1:n.152-1516del
NM_001318858.2:c.152-1516del	NP_001305787.1:n.152-1516del
NM_001318865.2:c.206+273del	NP_001305794.1:n.206+273del
NR_134890.2:n.340-1516del
NR_134891.2:n.243-1516del
NR_134892.2:n.243-966del
NR_134899.2:n.220+273del