Canonical Allele Identifier: CA1624303912

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961234_42961235delinsAG , CM000668.2:g.42961234_42961235delinsAG	GRCh38
NC_000006.11:g.42928972_42928973delinsAG , CM000668.1:g.42928972_42928973delinsAG	GRCh37
NC_000006.10:g.43036950_43036951delinsAG	NCBI36
NG_008396.1:g.5473_5474delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+261_206+262delinsAG MANE Select	ENSP00000361894.3:n.206+261_206+262delinsAG
ENST00000372808.3:c.206+261_206+262delinsAG	ENSP00000361894.3:n.206+261_206+262delinsAG
NM_018960.4:c.206+261_206+262delinsAG	NP_061833.1:n.206+261_206+262delinsAG
XM_011514493.1:c.-13-978_-13-977delinsAG	XP_011512795.1:n.-13-978_-13-977delinsAG
XM_011514494.1:c.-13-978_-13-977delinsAG	XP_011512796.1:n.-13-978_-13-977delinsAG
NM_001318856.1:c.9-978_9-977delinsAG	NP_001305785.1:n.9-978_9-977delinsAG
NM_001318857.1:c.152-1528_152-1527delinsAG	NP_001305786.1:n.152-1528_152-1527delinsAG
NM_001318858.1:c.152-1528_152-1527delinsAG	NP_001305787.1:n.152-1528_152-1527delinsAG
NM_001318865.1:c.206+261_206+262delinsAG	NP_001305794.1:n.206+261_206+262delinsAG
NM_018960.5:c.206+261_206+262delinsAG	NP_061833.1:n.206+261_206+262delinsAG
NR_134890.1:n.690-1528_690-1527delinsAG
NR_134891.1:n.593-1528_593-1527delinsAG
NR_134892.1:n.593-978_593-977delinsAG
NR_134899.1:n.220+261_220+262delinsAG
NM_018960.6:c.206+261_206+262delinsAG MANE Select	NP_061833.1:n.206+261_206+262delinsAG
NM_001318856.2:c.9-978_9-977delinsAG	NP_001305785.1:n.9-978_9-977delinsAG
NM_001318857.2:c.152-1528_152-1527delinsAG	NP_001305786.1:n.152-1528_152-1527delinsAG
NM_001318858.2:c.152-1528_152-1527delinsAG	NP_001305787.1:n.152-1528_152-1527delinsAG
NM_001318865.2:c.206+261_206+262delinsAG	NP_001305794.1:n.206+261_206+262delinsAG
NR_134890.2:n.340-1528_340-1527delinsAG
NR_134891.2:n.243-1528_243-1527delinsAG
NR_134892.2:n.243-978_243-977delinsAG
NR_134899.2:n.220+261_220+262delinsAG