Canonical Allele Identifier: CA2403795071

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282211_36282214delinsAAAG , CM000684.2:g.36282211_36282214delinsAAAG	GRCh38
NC_000022.10:g.36678257_36678260delinsAAAG , CM000684.1:g.36678257_36678260delinsAAAG	GRCh37
NC_000022.9:g.35008203_35008206delinsAAAG	NCBI36
NG_011884.2:g.110805_110808delinsCTTT , LRG_567:g.110805_110808delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2770_2773delinsCTTT
ENST00000685801.1:c.*454_*457delinsCTTT	ENSP00000510688.1:n.*454_*457delinsCTTT
ENST00000690244.1:n.1673_1676delinsCTTT
ENST00000691109.1:n.6632_6635delinsCTTT
ENST00000216181.11:c.*454_*457delinsCTTT MANE Select	ENSP00000216181.6:n.*454_*457delinsCTTT
ENST00000216181.9:c.*454_*457delinsCTTT	ENSP00000216181.5:n.*454_*457delinsCTTT
NM_002473.5:c.*454_*457delinsCTTT , LRG_567t1:c.*454_*457delinsCTTT	NP_002464.1:n.*454_*457delinsCTTT
XM_011530197.1:c.*454_*457delinsCTTT	XP_011528499.1:n.*454_*457delinsCTTT
XM_011530197.2:c.*454_*457delinsCTTT	XP_011528499.1:n.*454_*457delinsCTTT
XM_017028803.1:c.*454_*457delinsCTTT	XP_016884292.1:n.*454_*457delinsCTTT
XM_017028804.1:c.*454_*457delinsCTTT	XP_016884293.1:n.*454_*457delinsCTTT
XM_017028805.1:c.*454_*457delinsCTTT	XP_016884294.1:n.*454_*457delinsCTTT
XM_017028806.1:c.*454_*457delinsCTTT	XP_016884295.1:n.*454_*457delinsCTTT
NM_002473.6:c.*454_*457delinsCTTT MANE Select	NP_002464.1:n.*454_*457delinsCTTT