Canonical Allele Identifier: CA824892560

Gene: GNMT

Linked Data

• dbSNP Id: rs1467144840
• MyVariant Identifiers: chr6:g.42928978_42928981del (hg19) ; chr6:g.42961240_42961243del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961242_42961245del , CM000668.2:g.42961242_42961245del	GRCh38
NC_000006.11:g.42928980_42928983del , CM000668.1:g.42928980_42928983del	GRCh37
NC_000006.10:g.43036958_43036961del	NCBI36
NG_008396.1:g.5481_5484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+269_206+272del MANE Select	ENSP00000361894.3:n.206+269_206+272del
ENST00000372808.3:c.206+269_206+272del	ENSP00000361894.3:n.206+269_206+272del
NM_018960.4:c.206+269_206+272del	NP_061833.1:n.206+269_206+272del
XM_011514493.1:c.-13-970_-13-967del	XP_011512795.1:n.-13-970_-13-967del
XM_011514494.1:c.-13-970_-13-967del	XP_011512796.1:n.-13-970_-13-967del
NM_001318856.1:c.9-970_9-967del	NP_001305785.1:n.9-970_9-967del
NM_001318857.1:c.152-1520_152-1517del	NP_001305786.1:n.152-1520_152-1517del
NM_001318858.1:c.152-1520_152-1517del	NP_001305787.1:n.152-1520_152-1517del
NM_001318865.1:c.206+269_206+272del	NP_001305794.1:n.206+269_206+272del
NM_018960.5:c.206+269_206+272del	NP_061833.1:n.206+269_206+272del
NR_134890.1:n.690-1520_690-1517del
NR_134891.1:n.593-1520_593-1517del
NR_134892.1:n.593-970_593-967del
NR_134899.1:n.220+269_220+272del
NM_018960.6:c.206+269_206+272del MANE Select	NP_061833.1:n.206+269_206+272del
NM_001318856.2:c.9-970_9-967del	NP_001305785.1:n.9-970_9-967del
NM_001318857.2:c.152-1520_152-1517del	NP_001305786.1:n.152-1520_152-1517del
NM_001318858.2:c.152-1520_152-1517del	NP_001305787.1:n.152-1520_152-1517del
NM_001318865.2:c.206+269_206+272del	NP_001305794.1:n.206+269_206+272del
NR_134890.2:n.340-1520_340-1517del
NR_134891.2:n.243-1520_243-1517del
NR_134892.2:n.243-970_243-967del
NR_134899.2:n.220+269_220+272del