Canonical Allele Identifier: CA2403794985

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282068_36282069delinsAC , CM000684.2:g.36282068_36282069delinsAC	GRCh38
NC_000022.10:g.36678114_36678115delinsAC , CM000684.1:g.36678114_36678115delinsAC	GRCh37
NC_000022.9:g.35008060_35008061delinsAC	NCBI36
NG_011884.2:g.110950_110951delinsGT , LRG_567:g.110950_110951delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2915_2916delinsGT
ENST00000685801.1:c.*599_*600delinsGT	ENSP00000510688.1:n.*599_*600delinsGT
ENST00000690244.1:n.1818_1819delinsGT
ENST00000691109.1:n.6777_6778delinsGT
ENST00000216181.11:c.*599_*600delinsGT MANE Select	ENSP00000216181.6:n.*599_*600delinsGT
ENST00000216181.9:c.*599_*600delinsGT	ENSP00000216181.5:n.*599_*600delinsGT
NM_002473.5:c.*599_*600delinsGT , LRG_567t1:c.*599_*600delinsGT	NP_002464.1:n.*599_*600delinsGT
XM_011530197.1:c.*599_*600delinsGT	XP_011528499.1:n.*599_*600delinsGT
XM_011530197.2:c.*599_*600delinsGT	XP_011528499.1:n.*599_*600delinsGT
XM_017028803.1:c.*599_*600delinsGT	XP_016884292.1:n.*599_*600delinsGT
XM_017028804.1:c.*599_*600delinsGT	XP_016884293.1:n.*599_*600delinsGT
XM_017028805.1:c.*599_*600delinsGT	XP_016884294.1:n.*599_*600delinsGT
XM_017028806.1:c.*599_*600delinsGT	XP_016884295.1:n.*599_*600delinsGT
NM_002473.6:c.*599_*600delinsGT MANE Select	NP_002464.1:n.*599_*600delinsGT