Canonical Allele Identifier: CA1624303644

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960986_42960988delinsCGG , CM000668.2:g.42960986_42960988delinsCGG	GRCh38
NC_000006.11:g.42928724_42928726delinsCGG , CM000668.1:g.42928724_42928726delinsCGG	GRCh37
NC_000006.10:g.43036702_43036704delinsCGG	NCBI36
NG_008396.1:g.5225_5227delinsCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+13_206+15delinsCGG MANE Select	ENSP00000361894.3:n.206+13_206+15delinsCGG
ENST00000372808.3:c.206+13_206+15delinsCGG	ENSP00000361894.3:n.206+13_206+15delinsCGG
NM_018960.4:c.206+13_206+15delinsCGG	NP_061833.1:n.206+13_206+15delinsCGG
XM_011514493.1:c.-13-1226_-13-1224delinsCGG	XP_011512795.1:n.-13-1226_-13-1224delinsCGG
XM_011514494.1:c.-13-1226_-13-1224delinsCGG	XP_011512796.1:n.-13-1226_-13-1224delinsCGG
NM_001318856.1:c.9-1226_9-1224delinsCGG	NP_001305785.1:n.9-1226_9-1224delinsCGG
NM_001318857.1:c.152-1776_152-1774delinsCGG	NP_001305786.1:n.152-1776_152-1774delinsCGG
NM_001318858.1:c.152-1776_152-1774delinsCGG	NP_001305787.1:n.152-1776_152-1774delinsCGG
NM_001318865.1:c.206+13_206+15delinsCGG	NP_001305794.1:n.206+13_206+15delinsCGG
NM_018960.5:c.206+13_206+15delinsCGG	NP_061833.1:n.206+13_206+15delinsCGG
NR_134890.1:n.690-1776_690-1774delinsCGG
NR_134891.1:n.593-1776_593-1774delinsCGG
NR_134892.1:n.593-1226_593-1224delinsCGG
NR_134899.1:n.220+13_220+15delinsCGG
NM_018960.6:c.206+13_206+15delinsCGG MANE Select	NP_061833.1:n.206+13_206+15delinsCGG
NM_001318856.2:c.9-1226_9-1224delinsCGG	NP_001305785.1:n.9-1226_9-1224delinsCGG
NM_001318857.2:c.152-1776_152-1774delinsCGG	NP_001305786.1:n.152-1776_152-1774delinsCGG
NM_001318858.2:c.152-1776_152-1774delinsCGG	NP_001305787.1:n.152-1776_152-1774delinsCGG
NM_001318865.2:c.206+13_206+15delinsCGG	NP_001305794.1:n.206+13_206+15delinsCGG
NR_134890.2:n.340-1776_340-1774delinsCGG
NR_134891.2:n.243-1776_243-1774delinsCGG
NR_134892.2:n.243-1226_243-1224delinsCGG
NR_134899.2:n.220+13_220+15delinsCGG