Canonical Allele Identifier: CA2818872196

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282213del , CM000684.2:g.36282213del	GRCh38
NC_000022.10:g.36678259del , CM000684.1:g.36678259del	GRCh37
NC_000022.9:g.35008205del	NCBI36
NG_011884.2:g.110808del , LRG_567:g.110808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2773del
ENST00000685801.1:c.*457del	ENSP00000510688.1:n.*457del
ENST00000690244.1:n.1676del
ENST00000691109.1:n.6635del
ENST00000216181.11:c.*457del MANE Select	ENSP00000216181.6:n.*457del
ENST00000216181.9:c.*457del	ENSP00000216181.5:n.*457del
NM_002473.5:c.*457del , LRG_567t1:c.*457del	NP_002464.1:n.*457del
XM_011530197.1:c.*457del	XP_011528499.1:n.*457del
XM_011530197.2:c.*457del	XP_011528499.1:n.*457del
XM_017028803.1:c.*457del	XP_016884292.1:n.*457del
XM_017028804.1:c.*457del	XP_016884293.1:n.*457del
XM_017028805.1:c.*457del	XP_016884294.1:n.*457del
XM_017028806.1:c.*457del	XP_016884295.1:n.*457del
NM_002473.6:c.*457del MANE Select	NP_002464.1:n.*457del