Canonical Allele Identifier: CA2656433387

Gene: MYH9

Linked Data

• gnomAD v4: 22-36316794-G-GAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316801_36316805dup , CM000684.2:g.36316801_36316805dup	GRCh38
NC_000022.10:g.36712846_36712850dup , CM000684.1:g.36712846_36712850dup	GRCh37
NC_000022.9:g.35042792_35042796dup	NCBI36
NG_011884.2:g.76220_76224dup , LRG_567:g.76220_76224dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1442-130_1442-126dup
ENST00000685801.1:c.1228-130_1228-126dup	ENSP00000510688.1:n.1228-130_1228-126dup
ENST00000691109.1:n.1523-130_1523-126dup
ENST00000691687.1:n.2026-130_2026-126dup
ENST00000692930.1:n.1442-130_1442-126dup
ENST00000216181.11:c.1228-130_1228-126dup MANE Select	ENSP00000216181.6:n.1228-130_1228-126dup
ENST00000216181.9:c.1228-130_1228-126dup	ENSP00000216181.5:n.1228-130_1228-126dup
ENST00000477189.1:n.416-130_416-126dup
NM_002473.5:c.1228-130_1228-126dup , LRG_567t1:c.1228-130_1228-126dup	NP_002464.1:n.1228-130_1228-126dup
XM_011530197.1:c.1228-130_1228-126dup	XP_011528499.1:n.1228-130_1228-126dup
XM_011530197.2:c.1228-130_1228-126dup	XP_011528499.1:n.1228-130_1228-126dup
XM_017028803.1:c.1228-130_1228-126dup	XP_016884292.1:n.1228-130_1228-126dup
XM_017028804.1:c.1228-130_1228-126dup	XP_016884293.1:n.1228-130_1228-126dup
XM_017028805.1:c.1228-130_1228-126dup	XP_016884294.1:n.1228-130_1228-126dup
XM_017028806.1:c.1228-130_1228-126dup	XP_016884295.1:n.1228-130_1228-126dup
NM_002473.6:c.1228-130_1228-126dup MANE Select	NP_002464.1:n.1228-130_1228-126dup