Canonical Allele Identifier: CA2656433382

Gene: MYH9

Linked Data

• gnomAD v4: 22-36316794-GAAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316803_36316805del , CM000684.2:g.36316803_36316805del	GRCh38
NC_000022.10:g.36712848_36712850del , CM000684.1:g.36712848_36712850del	GRCh37
NC_000022.9:g.35042794_35042796del	NCBI36
NG_011884.2:g.76222_76224del , LRG_567:g.76222_76224del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1442-128_1442-126del
ENST00000685801.1:c.1228-128_1228-126del	ENSP00000510688.1:n.1228-128_1228-126del
ENST00000691109.1:n.1523-128_1523-126del
ENST00000691687.1:n.2026-128_2026-126del
ENST00000692930.1:n.1442-128_1442-126del
ENST00000216181.11:c.1228-128_1228-126del MANE Select	ENSP00000216181.6:n.1228-128_1228-126del
ENST00000216181.9:c.1228-128_1228-126del	ENSP00000216181.5:n.1228-128_1228-126del
ENST00000477189.1:n.416-128_416-126del
NM_002473.5:c.1228-128_1228-126del , LRG_567t1:c.1228-128_1228-126del	NP_002464.1:n.1228-128_1228-126del
XM_011530197.1:c.1228-128_1228-126del	XP_011528499.1:n.1228-128_1228-126del
XM_011530197.2:c.1228-128_1228-126del	XP_011528499.1:n.1228-128_1228-126del
XM_017028803.1:c.1228-128_1228-126del	XP_016884292.1:n.1228-128_1228-126del
XM_017028804.1:c.1228-128_1228-126del	XP_016884293.1:n.1228-128_1228-126del
XM_017028805.1:c.1228-128_1228-126del	XP_016884294.1:n.1228-128_1228-126del
XM_017028806.1:c.1228-128_1228-126del	XP_016884295.1:n.1228-128_1228-126del
NM_002473.6:c.1228-128_1228-126del MANE Select	NP_002464.1:n.1228-128_1228-126del