Canonical Allele Identifier: CA1624303918

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961240_42961241delinsAG , CM000668.2:g.42961240_42961241delinsAG	GRCh38
NC_000006.11:g.42928978_42928979delinsAG , CM000668.1:g.42928978_42928979delinsAG	GRCh37
NC_000006.10:g.43036956_43036957delinsAG	NCBI36
NG_008396.1:g.5479_5480delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+267_206+268delinsAG MANE Select	ENSP00000361894.3:n.206+267_206+268delinsAG
ENST00000372808.3:c.206+267_206+268delinsAG	ENSP00000361894.3:n.206+267_206+268delinsAG
NM_018960.4:c.206+267_206+268delinsAG	NP_061833.1:n.206+267_206+268delinsAG
XM_011514493.1:c.-13-972_-13-971delinsAG	XP_011512795.1:n.-13-972_-13-971delinsAG
XM_011514494.1:c.-13-972_-13-971delinsAG	XP_011512796.1:n.-13-972_-13-971delinsAG
NM_001318856.1:c.9-972_9-971delinsAG	NP_001305785.1:n.9-972_9-971delinsAG
NM_001318857.1:c.152-1522_152-1521delinsAG	NP_001305786.1:n.152-1522_152-1521delinsAG
NM_001318858.1:c.152-1522_152-1521delinsAG	NP_001305787.1:n.152-1522_152-1521delinsAG
NM_001318865.1:c.206+267_206+268delinsAG	NP_001305794.1:n.206+267_206+268delinsAG
NM_018960.5:c.206+267_206+268delinsAG	NP_061833.1:n.206+267_206+268delinsAG
NR_134890.1:n.690-1522_690-1521delinsAG
NR_134891.1:n.593-1522_593-1521delinsAG
NR_134892.1:n.593-972_593-971delinsAG
NR_134899.1:n.220+267_220+268delinsAG
NM_018960.6:c.206+267_206+268delinsAG MANE Select	NP_061833.1:n.206+267_206+268delinsAG
NM_001318856.2:c.9-972_9-971delinsAG	NP_001305785.1:n.9-972_9-971delinsAG
NM_001318857.2:c.152-1522_152-1521delinsAG	NP_001305786.1:n.152-1522_152-1521delinsAG
NM_001318858.2:c.152-1522_152-1521delinsAG	NP_001305787.1:n.152-1522_152-1521delinsAG
NM_001318865.2:c.206+267_206+268delinsAG	NP_001305794.1:n.206+267_206+268delinsAG
NR_134890.2:n.340-1522_340-1521delinsAG
NR_134891.2:n.243-1522_243-1521delinsAG
NR_134892.2:n.243-972_243-971delinsAG
NR_134899.2:n.220+267_220+268delinsAG