Canonical Allele Identifier: CA2403795042

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282166_36282174delinsAAGGGGCAG , CM000684.2:g.36282166_36282174delinsAAGGGGCAG	GRCh38
NC_000022.10:g.36678212_36678220delinsAAGGGGCAG , CM000684.1:g.36678212_36678220delinsAAGGGGCAG	GRCh37
NC_000022.9:g.35008158_35008166delinsAAGGGGCAG	NCBI36
NG_011884.2:g.110845_110853delinsCTGCCCCTT , LRG_567:g.110845_110853delinsCTGCCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2810_2818delinsCTGCCCCTT
ENST00000685801.1:c.*494_*502delinsCTGCCCCTT	ENSP00000510688.1:n.*494_*502delinsCTGCCCCTT
ENST00000690244.1:n.1713_1721delinsCTGCCCCTT
ENST00000691109.1:n.6672_6680delinsCTGCCCCTT
ENST00000216181.11:c.*494_*502delinsCTGCCCCTT MANE Select	ENSP00000216181.6:n.*494_*502delinsCTGCCCCTT
ENST00000216181.9:c.*494_*502delinsCTGCCCCTT	ENSP00000216181.5:n.*494_*502delinsCTGCCCCTT
NM_002473.5:c.*494_*502delinsCTGCCCCTT , LRG_567t1:c.*494_*502delinsCTGCCCCTT	NP_002464.1:n.*494_*502delinsCTGCCCCTT
XM_011530197.1:c.*494_*502delinsCTGCCCCTT	XP_011528499.1:n.*494_*502delinsCTGCCCCTT
XM_011530197.2:c.*494_*502delinsCTGCCCCTT	XP_011528499.1:n.*494_*502delinsCTGCCCCTT
XM_017028803.1:c.*494_*502delinsCTGCCCCTT	XP_016884292.1:n.*494_*502delinsCTGCCCCTT
XM_017028804.1:c.*494_*502delinsCTGCCCCTT	XP_016884293.1:n.*494_*502delinsCTGCCCCTT
XM_017028805.1:c.*494_*502delinsCTGCCCCTT	XP_016884294.1:n.*494_*502delinsCTGCCCCTT
XM_017028806.1:c.*494_*502delinsCTGCCCCTT	XP_016884295.1:n.*494_*502delinsCTGCCCCTT
NM_002473.6:c.*494_*502delinsCTGCCCCTT MANE Select	NP_002464.1:n.*494_*502delinsCTGCCCCTT