Canonical Allele Identifier: CA639148293

Gene: MYH9

Linked Data

• dbSNP Id: rs1160312752
• gnomAD v2: 22-36678257-AAAG-A
• gnomAD v3: 22-36282211-AAAG-A
• gnomAD v4: 22-36282211-AAAG-A
• MyVariant Identifiers: chr22:g.36678258_36678260del (hg19) ; chr22:g.36282212_36282214del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282214_36282216del , CM000684.2:g.36282214_36282216del	GRCh38
NC_000022.10:g.36678260_36678262del , CM000684.1:g.36678260_36678262del	GRCh37
NC_000022.9:g.35008206_35008208del	NCBI36
NG_011884.2:g.110805_110807del , LRG_567:g.110805_110807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2770_2772del
ENST00000685801.1:c.*454_*456del	ENSP00000510688.1:n.*454_*456del
ENST00000690244.1:n.1673_1675del
ENST00000691109.1:n.6632_6634del
ENST00000216181.11:c.*454_*456del MANE Select	ENSP00000216181.6:n.*454_*456del
ENST00000216181.9:c.*454_*456del	ENSP00000216181.5:n.*454_*456del
NM_002473.5:c.*454_*456del , LRG_567t1:c.*454_*456del	NP_002464.1:n.*454_*456del
XM_011530197.1:c.*454_*456del	XP_011528499.1:n.*454_*456del
XM_011530197.2:c.*454_*456del	XP_011528499.1:n.*454_*456del
XM_017028803.1:c.*454_*456del	XP_016884292.1:n.*454_*456del
XM_017028804.1:c.*454_*456del	XP_016884293.1:n.*454_*456del
XM_017028805.1:c.*454_*456del	XP_016884294.1:n.*454_*456del
XM_017028806.1:c.*454_*456del	XP_016884295.1:n.*454_*456del
NM_002473.6:c.*454_*456del MANE Select	NP_002464.1:n.*454_*456del