Canonical Allele Identifier: CA2403795004

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282100_36282102delinsGCA , CM000684.2:g.36282100_36282102delinsGCA	GRCh38
NC_000022.10:g.36678146_36678148delinsGCA , CM000684.1:g.36678146_36678148delinsGCA	GRCh37
NC_000022.9:g.35008092_35008094delinsGCA	NCBI36
NG_011884.2:g.110917_110919delinsTGC , LRG_567:g.110917_110919delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2882_2884delinsTGC
ENST00000685801.1:c.*566_*568delinsTGC	ENSP00000510688.1:n.*566_*568delinsTGC
ENST00000690244.1:n.1785_1787delinsTGC
ENST00000691109.1:n.6744_6746delinsTGC
ENST00000216181.11:c.*566_*568delinsTGC MANE Select	ENSP00000216181.6:n.*566_*568delinsTGC
ENST00000216181.9:c.*566_*568delinsTGC	ENSP00000216181.5:n.*566_*568delinsTGC
NM_002473.5:c.*566_*568delinsTGC , LRG_567t1:c.*566_*568delinsTGC	NP_002464.1:n.*566_*568delinsTGC
XM_011530197.1:c.*566_*568delinsTGC	XP_011528499.1:n.*566_*568delinsTGC
XM_011530197.2:c.*566_*568delinsTGC	XP_011528499.1:n.*566_*568delinsTGC
XM_017028803.1:c.*566_*568delinsTGC	XP_016884292.1:n.*566_*568delinsTGC
XM_017028804.1:c.*566_*568delinsTGC	XP_016884293.1:n.*566_*568delinsTGC
XM_017028805.1:c.*566_*568delinsTGC	XP_016884294.1:n.*566_*568delinsTGC
XM_017028806.1:c.*566_*568delinsTGC	XP_016884295.1:n.*566_*568delinsTGC
NM_002473.6:c.*566_*568delinsTGC MANE Select	NP_002464.1:n.*566_*568delinsTGC