Canonical Allele Identifier: CA2403795074

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282216_36282219delinsAAGG , CM000684.2:g.36282216_36282219delinsAAGG	GRCh38
NC_000022.10:g.36678262_36678265delinsAAGG , CM000684.1:g.36678262_36678265delinsAAGG	GRCh37
NC_000022.9:g.35008208_35008211delinsAAGG	NCBI36
NG_011884.2:g.110800_110803delinsCCTT , LRG_567:g.110800_110803delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2765_2768delinsCCTT
ENST00000685801.1:c.*449_*452delinsCCTT	ENSP00000510688.1:n.*449_*452delinsCCTT
ENST00000690244.1:n.1668_1671delinsCCTT
ENST00000691109.1:n.6627_6630delinsCCTT
ENST00000216181.11:c.*449_*452delinsCCTT MANE Select	ENSP00000216181.6:n.*449_*452delinsCCTT
ENST00000216181.9:c.*449_*452delinsCCTT	ENSP00000216181.5:n.*449_*452delinsCCTT
NM_002473.5:c.*449_*452delinsCCTT , LRG_567t1:c.*449_*452delinsCCTT	NP_002464.1:n.*449_*452delinsCCTT
XM_011530197.1:c.*449_*452delinsCCTT	XP_011528499.1:n.*449_*452delinsCCTT
XM_011530197.2:c.*449_*452delinsCCTT	XP_011528499.1:n.*449_*452delinsCCTT
XM_017028803.1:c.*449_*452delinsCCTT	XP_016884292.1:n.*449_*452delinsCCTT
XM_017028804.1:c.*449_*452delinsCCTT	XP_016884293.1:n.*449_*452delinsCCTT
XM_017028805.1:c.*449_*452delinsCCTT	XP_016884294.1:n.*449_*452delinsCCTT
XM_017028806.1:c.*449_*452delinsCCTT	XP_016884295.1:n.*449_*452delinsCCTT
NM_002473.6:c.*449_*452delinsCCTT MANE Select	NP_002464.1:n.*449_*452delinsCCTT