Canonical Allele Identifier: CA1624303891

Gene: GNMT

Linked Data

• dbSNP Id: rs1769370404

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961211_42961212del , CM000668.2:g.42961211_42961212del	GRCh38
NC_000006.11:g.42928949_42928950del , CM000668.1:g.42928949_42928950del	GRCh37
NC_000006.10:g.43036927_43036928del	NCBI36
NG_008396.1:g.5450_5451del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+238_206+239del MANE Select	ENSP00000361894.3:n.206+238_206+239del
ENST00000372808.3:c.206+238_206+239del	ENSP00000361894.3:n.206+238_206+239del
NM_018960.4:c.206+238_206+239del	NP_061833.1:n.206+238_206+239del
XM_011514493.1:c.-13-1001_-13-1000del	XP_011512795.1:n.-13-1001_-13-1000del
XM_011514494.1:c.-13-1001_-13-1000del	XP_011512796.1:n.-13-1001_-13-1000del
NM_001318856.1:c.9-1001_9-1000del	NP_001305785.1:n.9-1001_9-1000del
NM_001318857.1:c.152-1551_152-1550del	NP_001305786.1:n.152-1551_152-1550del
NM_001318858.1:c.152-1551_152-1550del	NP_001305787.1:n.152-1551_152-1550del
NM_001318865.1:c.206+238_206+239del	NP_001305794.1:n.206+238_206+239del
NM_018960.5:c.206+238_206+239del	NP_061833.1:n.206+238_206+239del
NR_134890.1:n.690-1551_690-1550del
NR_134891.1:n.593-1551_593-1550del
NR_134892.1:n.593-1001_593-1000del
NR_134899.1:n.220+238_220+239del
NM_018960.6:c.206+238_206+239del MANE Select	NP_061833.1:n.206+238_206+239del
NM_001318856.2:c.9-1001_9-1000del	NP_001305785.1:n.9-1001_9-1000del
NM_001318857.2:c.152-1551_152-1550del	NP_001305786.1:n.152-1551_152-1550del
NM_001318858.2:c.152-1551_152-1550del	NP_001305787.1:n.152-1551_152-1550del
NM_001318865.2:c.206+238_206+239del	NP_001305794.1:n.206+238_206+239del
NR_134890.2:n.340-1551_340-1550del
NR_134891.2:n.243-1551_243-1550del
NR_134892.2:n.243-1001_243-1000del
NR_134899.2:n.220+238_220+239del