Canonical Allele Identifier: CA257099

Gene: MYH9

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282733del , CM000684.2:g.36282733del	GRCh38
NC_000022.10:g.36678779del , CM000684.1:g.36678779del	GRCh37
NC_000022.9:g.35008725del	NCBI36
NG_011884.2:g.110289del , LRG_567:g.110289del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2254del
ENST00000685801.1:c.5884del	ENSP00000510688.1:p.Asp1962MetfsTer7
ENST00000690244.1:n.1157del
ENST00000691109.1:n.6116del
ENST00000216181.11:c.5821del MANE Select	ENSP00000216181.6:p.Asp1941MetfsTer7
ENST00000216181.9:c.5821del	ENSP00000216181.5:p.Asp1941MetfsTer7
NM_002473.5:c.5821del , LRG_567t1:c.5821del	NP_002464.1:p.Asp1941MetfsTer7
XM_011530197.1:c.5821del	XP_011528499.1:p.Asp1941MetfsTer7
XM_011530197.2:c.5821del	XP_011528499.1:p.Asp1941MetfsTer7
XM_017028803.1:c.5821del	XP_016884292.1:p.Asp1941MetfsTer7
XM_017028804.1:c.5821del	XP_016884293.1:p.Asp1941MetfsTer7
XM_017028805.1:c.5821del	XP_016884294.1:p.Asp1941MetfsTer7
XM_017028806.1:c.5821del	XP_016884295.1:p.Asp1941MetfsTer7
NM_002473.6:c.5821del MANE Select	NP_002464.1:p.Asp1941MetfsTer7