Canonical Allele Identifier: CA215989569

Gene: MGMT

Linked Data

• dbSNP Id: rs932993888
• gnomAD v3: 10-129468194-TG-T
• gnomAD v4: 10-129468194-TG-T
• MyVariant Identifiers: chr10:g.131266459del (hg19) ; chr10:g.129468195del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468197del , CM000672.2:g.129468197del	GRCh38
NC_000010.10:g.131266461del , CM000672.1:g.131266461del	GRCh37
NC_000010.9:g.131156451del	NCBI36
NG_052673.1:g.6014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.81+901del	ENSP00000302111.7:n.81+901del
ENST00000651593.1:c.-13+901del MANE Select	ENSP00000498729.1:n.-13+901del
ENST00000306010.7:c.81+901del	ENSP00000302111.7:n.81+901del
ENST00000482547.1:n.35+901del
ENST00000482653.1:n.68+901del
NM_002412.3:c.81+901del	NP_002403.2:n.81+901del
NM_002412.4:c.81+901del	NP_002403.2:n.81+901del
XM_005252682.2:c.-13+756del	XP_005252739.1:n.-13+756del
NM_002412.5:c.-13+901del MANE Select	NP_002403.3:n.-13+901del