Canonical Allele Identifier: CA2403794874

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281844_36281845delinsTG , CM000684.2:g.36281844_36281845delinsTG	GRCh38
NC_000022.10:g.36677890_36677891delinsTG , CM000684.1:g.36677890_36677891delinsTG	GRCh37
NC_000022.9:g.35007836_35007837delinsTG	NCBI36
NG_011884.2:g.111174_111175delinsCA , LRG_567:g.111174_111175delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000685708.1:n.3139_3140delinsCA
ENST00000685801.1:c.*823_*824delinsCA	ENSP00000510688.1:n.*823_*824delinsCA
ENST00000690244.1:n.2042_2043delinsCA
ENST00000691109.1:n.7001_7002delinsCA
ENST00000216181.11:c.*823_*824delinsCA MANE Select	ENSP00000216181.6:n.*823_*824delinsCA
ENST00000216181.9:c.*823_*824delinsCA	ENSP00000216181.5:n.*823_*824delinsCA
NM_002473.5:c.*823_*824delinsCA , LRG_567t1:c.*823_*824delinsCA	NP_002464.1:n.*823_*824delinsCA
XM_011530197.1:c.*823_*824delinsCA	XP_011528499.1:n.*823_*824delinsCA
XM_011530197.2:c.*823_*824delinsCA	XP_011528499.1:n.*823_*824delinsCA
XM_017028803.1:c.*823_*824delinsCA	XP_016884292.1:n.*823_*824delinsCA
XM_017028804.1:c.*823_*824delinsCA	XP_016884293.1:n.*823_*824delinsCA
XM_017028805.1:c.*823_*824delinsCA	XP_016884294.1:n.*823_*824delinsCA
XM_017028806.1:c.*823_*824delinsCA	XP_016884295.1:n.*823_*824delinsCA
NM_002473.6:c.*823_*824delinsCA MANE Select	NP_002464.1:n.*823_*824delinsCA