Canonical Allele Identifier: CA658254027

Gene: MYH9

Linked Data

• COSMIC: COSN19521963

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281786_36281787insC , CM000684.2:g.36281786_36281787insC	GRCh38
NC_000022.10:g.36677832_36677833insC , CM000684.1:g.36677832_36677833insC	GRCh37
NC_000022.9:g.35007778_35007779insC	NCBI36
NG_011884.2:g.111232_111233insG , LRG_567:g.111232_111233insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3197_3198insG
ENST00000685801.1:c.*881_*882insG	ENSP00000510688.1:n.*881_*882insG
ENST00000690244.1:n.2100_2101insG
ENST00000691109.1:n.7059_7060insG
ENST00000216181.11:c.*881_*882insG MANE Select	ENSP00000216181.6:n.*881_*882insG
ENST00000216181.9:c.*881_*882insG	ENSP00000216181.5:n.*881_*882insG
NM_002473.5:c.*881_*882insG , LRG_567t1:c.*881_*882insG	NP_002464.1:n.*881_*882insG
XM_011530197.1:c.*881_*882insG	XP_011528499.1:n.*881_*882insG
XM_011530197.2:c.*881_*882insG	XP_011528499.1:n.*881_*882insG
XM_017028803.1:c.*881_*882insG	XP_016884292.1:n.*881_*882insG
XM_017028804.1:c.*881_*882insG	XP_016884293.1:n.*881_*882insG
XM_017028805.1:c.*881_*882insG	XP_016884294.1:n.*881_*882insG
XM_017028806.1:c.*881_*882insG	XP_016884295.1:n.*881_*882insG
NM_002473.6:c.*881_*882insG MANE Select	NP_002464.1:n.*881_*882insG