Canonical Allele Identifier: CA2678789463

Gene: GNMT

Linked Data

• gnomAD v4: 6-42960722-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960723_42960724del , CM000668.2:g.42960723_42960724del	GRCh38
NC_000006.11:g.42928461_42928462del , CM000668.1:g.42928461_42928462del	GRCh37
NC_000006.10:g.43036439_43036440del	NCBI36
NG_008396.1:g.4962_4963del

Transcript Alleles

HGVS	Amino-acid Change
XM_011514493.1:c.-13-1489_-13-1488del	XP_011512795.1:n.-13-1489_-13-1488del
XM_011514494.1:c.-13-1489_-13-1488del	XP_011512796.1:n.-13-1489_-13-1488del
NM_001318856.1:c.9-1489_9-1488del	NP_001305785.1:n.9-1489_9-1488del
NM_001318857.1:c.152-2039_152-2038del	NP_001305786.1:n.152-2039_152-2038del
NM_001318858.1:c.152-2039_152-2038del	NP_001305787.1:n.152-2039_152-2038del
NR_134890.1:n.690-2039_690-2038del
NR_134891.1:n.593-2039_593-2038del
NR_134892.1:n.593-1489_593-1488del
NM_001318856.2:c.9-1489_9-1488del	NP_001305785.1:n.9-1489_9-1488del
NM_001318857.2:c.152-2039_152-2038del	NP_001305786.1:n.152-2039_152-2038del
NM_001318858.2:c.152-2039_152-2038del	NP_001305787.1:n.152-2039_152-2038del
NR_134890.2:n.340-2039_340-2038del
NR_134891.2:n.243-2039_243-2038del
NR_134892.2:n.243-1489_243-1488del