Canonical Allele Identifier: CA2403795005

Gene: MYH9

Linked Data

• dbSNP Id: rs2016499357

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282103_36282104del , CM000684.2:g.36282103_36282104del	GRCh38
NC_000022.10:g.36678149_36678150del , CM000684.1:g.36678149_36678150del	GRCh37
NC_000022.9:g.35008095_35008096del	NCBI36
NG_011884.2:g.110917_110918del , LRG_567:g.110917_110918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2882_2883del
ENST00000685801.1:c.*566_*567del	ENSP00000510688.1:n.*566_*567del
ENST00000690244.1:n.1785_1786del
ENST00000691109.1:n.6744_6745del
ENST00000216181.11:c.*566_*567del MANE Select	ENSP00000216181.6:n.*566_*567del
ENST00000216181.9:c.*566_*567del	ENSP00000216181.5:n.*566_*567del
NM_002473.5:c.*566_*567del , LRG_567t1:c.*566_*567del	NP_002464.1:n.*566_*567del
XM_011530197.1:c.*566_*567del	XP_011528499.1:n.*566_*567del
XM_011530197.2:c.*566_*567del	XP_011528499.1:n.*566_*567del
XM_017028803.1:c.*566_*567del	XP_016884292.1:n.*566_*567del
XM_017028804.1:c.*566_*567del	XP_016884293.1:n.*566_*567del
XM_017028805.1:c.*566_*567del	XP_016884294.1:n.*566_*567del
XM_017028806.1:c.*566_*567del	XP_016884295.1:n.*566_*567del
NM_002473.6:c.*566_*567del MANE Select	NP_002464.1:n.*566_*567del