Canonical Allele Identifier: CA2656426315

Gene: MYH9

Linked Data

• gnomAD v4: 22-36281919-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281922del , CM000684.2:g.36281922del	GRCh38
NC_000022.10:g.36677968del , CM000684.1:g.36677968del	GRCh37
NC_000022.9:g.35007914del	NCBI36
NG_011884.2:g.111099del , LRG_567:g.111099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3064del
ENST00000685801.1:c.*748del	ENSP00000510688.1:n.*748del
ENST00000690244.1:n.1967del
ENST00000691109.1:n.6926del
ENST00000216181.11:c.*748del MANE Select	ENSP00000216181.6:n.*748del
ENST00000216181.9:c.*748del	ENSP00000216181.5:n.*748del
NM_002473.5:c.*748del , LRG_567t1:c.*748del	NP_002464.1:n.*748del
XM_011530197.1:c.*748del	XP_011528499.1:n.*748del
XM_011530197.2:c.*748del	XP_011528499.1:n.*748del
XM_017028803.1:c.*748del	XP_016884292.1:n.*748del
XM_017028804.1:c.*748del	XP_016884293.1:n.*748del
XM_017028805.1:c.*748del	XP_016884294.1:n.*748del
XM_017028806.1:c.*748del	XP_016884295.1:n.*748del
NM_002473.6:c.*748del MANE Select	NP_002464.1:n.*748del