Canonical Allele Identifier: CA2678789526

Gene: GNMT

Linked Data

• gnomAD v4: 6-42960767-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960767G>T , CM000668.2:g.42960767G>T	GRCh38
NC_000006.11:g.42928505G>T , CM000668.1:g.42928505G>T	GRCh37
NC_000006.10:g.43036483G>T	NCBI36
NG_008396.1:g.5006G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.-1G>T MANE Select	ENSP00000361894.3:n.-1G>T
ENST00000372808.3:c.-1G>T	ENSP00000361894.3:n.-1G>T
NM_018960.4:c.-1G>T	NP_061833.1:n.-1G>T
XM_011514493.1:c.-13-1445G>T	XP_011512795.1:n.-13-1445G>T
XM_011514494.1:c.-13-1445G>T	XP_011512796.1:n.-13-1445G>T
NM_001318856.1:c.9-1445G>T	NP_001305785.1:n.9-1445G>T
NM_001318857.1:c.152-1995G>T	NP_001305786.1:n.152-1995G>T
NM_001318858.1:c.152-1995G>T	NP_001305787.1:n.152-1995G>T
NM_001318865.1:c.-1G>T	NP_001305794.1:n.-1G>T
NM_018960.5:c.-1G>T	NP_061833.1:n.-1G>T
NR_134890.1:n.690-1995G>T
NR_134891.1:n.593-1995G>T
NR_134892.1:n.593-1445G>T
NR_134899.1:n.14G>T
NM_018960.6:c.-1G>T MANE Select	NP_061833.1:n.-1G>T
NM_001318856.2:c.9-1445G>T	NP_001305785.1:n.9-1445G>T
NM_001318857.2:c.152-1995G>T	NP_001305786.1:n.152-1995G>T
NM_001318858.2:c.152-1995G>T	NP_001305787.1:n.152-1995G>T
NM_001318865.2:c.-1G>T	NP_001305794.1:n.-1G>T
NR_134890.2:n.340-1995G>T
NR_134891.2:n.243-1995G>T
NR_134892.2:n.243-1445G>T
NR_134899.2:n.14G>T