Canonical Allele Identifier: CA2403794835

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281775_36281776delinsCA , CM000684.2:g.36281775_36281776delinsCA	GRCh38
NC_000022.10:g.36677821_36677822delinsCA , CM000684.1:g.36677821_36677822delinsCA	GRCh37
NC_000022.9:g.35007767_35007768delinsCA	NCBI36
NG_011884.2:g.111243_111244delinsTG , LRG_567:g.111243_111244delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3208_3209delinsTG
ENST00000685801.1:c.*892_*893delinsTG	ENSP00000510688.1:n.*892_*893delinsTG
ENST00000690244.1:n.2111_2112delinsTG
ENST00000691109.1:n.7070_7071delinsTG
ENST00000216181.11:c.*892_*893delinsTG MANE Select	ENSP00000216181.6:n.*892_*893delinsTG
ENST00000216181.9:c.*892_*893delinsTG	ENSP00000216181.5:n.*892_*893delinsTG
NM_002473.5:c.*892_*893delinsTG , LRG_567t1:c.*892_*893delinsTG	NP_002464.1:n.*892_*893delinsTG
XM_011530197.1:c.*892_*893delinsTG	XP_011528499.1:n.*892_*893delinsTG
XM_011530197.2:c.*892_*893delinsTG	XP_011528499.1:n.*892_*893delinsTG
XM_017028803.1:c.*892_*893delinsTG	XP_016884292.1:n.*892_*893delinsTG
XM_017028804.1:c.*892_*893delinsTG	XP_016884293.1:n.*892_*893delinsTG
XM_017028805.1:c.*892_*893delinsTG	XP_016884294.1:n.*892_*893delinsTG
XM_017028806.1:c.*892_*893delinsTG	XP_016884295.1:n.*892_*893delinsTG
NM_002473.6:c.*892_*893delinsTG MANE Select	NP_002464.1:n.*892_*893delinsTG