Canonical Allele Identifier: CA2403794855

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281814_36281816delinsTGG , CM000684.2:g.36281814_36281816delinsTGG	GRCh38
NC_000022.10:g.36677860_36677862delinsTGG , CM000684.1:g.36677860_36677862delinsTGG	GRCh37
NC_000022.9:g.35007806_35007808delinsTGG	NCBI36
NG_011884.2:g.111203_111205delinsCCA , LRG_567:g.111203_111205delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3168_3170delinsCCA
ENST00000685801.1:c.*852_*854delinsCCA	ENSP00000510688.1:n.*852_*854delinsCCA
ENST00000690244.1:n.2071_2073delinsCCA
ENST00000691109.1:n.7030_7032delinsCCA
ENST00000216181.11:c.*852_*854delinsCCA MANE Select	ENSP00000216181.6:n.*852_*854delinsCCA
ENST00000216181.9:c.*852_*854delinsCCA	ENSP00000216181.5:n.*852_*854delinsCCA
NM_002473.5:c.*852_*854delinsCCA , LRG_567t1:c.*852_*854delinsCCA	NP_002464.1:n.*852_*854delinsCCA
XM_011530197.1:c.*852_*854delinsCCA	XP_011528499.1:n.*852_*854delinsCCA
XM_011530197.2:c.*852_*854delinsCCA	XP_011528499.1:n.*852_*854delinsCCA
XM_017028803.1:c.*852_*854delinsCCA	XP_016884292.1:n.*852_*854delinsCCA
XM_017028804.1:c.*852_*854delinsCCA	XP_016884293.1:n.*852_*854delinsCCA
XM_017028805.1:c.*852_*854delinsCCA	XP_016884294.1:n.*852_*854delinsCCA
XM_017028806.1:c.*852_*854delinsCCA	XP_016884295.1:n.*852_*854delinsCCA
NM_002473.6:c.*852_*854delinsCCA MANE Select	NP_002464.1:n.*852_*854delinsCCA