Canonical Allele Identifier: CA2656426492

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282073-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282078_36282079del , CM000684.2:g.36282078_36282079del	GRCh38
NC_000022.10:g.36678124_36678125del , CM000684.1:g.36678124_36678125del	GRCh37
NC_000022.9:g.35008070_35008071del	NCBI36
NG_011884.2:g.110944_110945del , LRG_567:g.110944_110945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2909_2910del
ENST00000685801.1:c.*593_*594del	ENSP00000510688.1:n.*593_*594del
ENST00000690244.1:n.1812_1813del
ENST00000691109.1:n.6771_6772del
ENST00000216181.11:c.*593_*594del MANE Select	ENSP00000216181.6:n.*593_*594del
ENST00000216181.9:c.*593_*594del	ENSP00000216181.5:n.*593_*594del
NM_002473.5:c.*593_*594del , LRG_567t1:c.*593_*594del	NP_002464.1:n.*593_*594del
XM_011530197.1:c.*593_*594del	XP_011528499.1:n.*593_*594del
XM_011530197.2:c.*593_*594del	XP_011528499.1:n.*593_*594del
XM_017028803.1:c.*593_*594del	XP_016884292.1:n.*593_*594del
XM_017028804.1:c.*593_*594del	XP_016884293.1:n.*593_*594del
XM_017028805.1:c.*593_*594del	XP_016884294.1:n.*593_*594del
XM_017028806.1:c.*593_*594del	XP_016884295.1:n.*593_*594del
NM_002473.6:c.*593_*594del MANE Select	NP_002464.1:n.*593_*594del