Canonical Allele Identifier: CA658254039

Gene: MYH9

Linked Data

• COSMIC: COSN21569802

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282241_36282242insA , CM000684.2:g.36282241_36282242insA	GRCh38
NC_000022.10:g.36678287_36678288insA , CM000684.1:g.36678287_36678288insA	GRCh37
NC_000022.9:g.35008233_35008234insA	NCBI36
NG_011884.2:g.110777_110778insT , LRG_567:g.110777_110778insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2742_2743insT
ENST00000685801.1:c.*426_*427insT	ENSP00000510688.1:n.*426_*427insT
ENST00000690244.1:n.1645_1646insT
ENST00000691109.1:n.6604_6605insT
ENST00000216181.11:c.*426_*427insT MANE Select	ENSP00000216181.6:n.*426_*427insT
ENST00000216181.9:c.*426_*427insT	ENSP00000216181.5:n.*426_*427insT
NM_002473.5:c.*426_*427insT , LRG_567t1:c.*426_*427insT	NP_002464.1:n.*426_*427insT
XM_011530197.1:c.*426_*427insT	XP_011528499.1:n.*426_*427insT
XM_011530197.2:c.*426_*427insT	XP_011528499.1:n.*426_*427insT
XM_017028803.1:c.*426_*427insT	XP_016884292.1:n.*426_*427insT
XM_017028804.1:c.*426_*427insT	XP_016884293.1:n.*426_*427insT
XM_017028805.1:c.*426_*427insT	XP_016884294.1:n.*426_*427insT
XM_017028806.1:c.*426_*427insT	XP_016884295.1:n.*426_*427insT
NM_002473.6:c.*426_*427insT MANE Select	NP_002464.1:n.*426_*427insT