Canonical Allele Identifier: CA2656426596

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282151-GGGAGTGGGAGGCCCAAGGGGCAGAGGTGTGTGAGGTCACCACGTGTGATTGCAAACAGCAAAGAAAGGAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282160_36282231del , CM000684.2:g.36282160_36282231del	GRCh38
NC_000022.10:g.36678206_36678277del , CM000684.1:g.36678206_36678277del	GRCh37
NC_000022.9:g.35008152_35008223del	NCBI36
NG_011884.2:g.110796_110867del , LRG_567:g.110796_110867del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2761_2832del
ENST00000685801.1:c.*445_*516del	ENSP00000510688.1:n.*445_*516del
ENST00000690244.1:n.1664_1735del
ENST00000691109.1:n.6623_6694del
ENST00000216181.11:c.*445_*516del MANE Select	ENSP00000216181.6:n.*445_*516del
ENST00000216181.9:c.*445_*516del	ENSP00000216181.5:n.*445_*516del
NM_002473.5:c.*445_*516del , LRG_567t1:c.*445_*516del	NP_002464.1:n.*445_*516del
XM_011530197.1:c.*445_*516del	XP_011528499.1:n.*445_*516del
XM_011530197.2:c.*445_*516del	XP_011528499.1:n.*445_*516del
XM_017028803.1:c.*445_*516del	XP_016884292.1:n.*445_*516del
XM_017028804.1:c.*445_*516del	XP_016884293.1:n.*445_*516del
XM_017028805.1:c.*445_*516del	XP_016884294.1:n.*445_*516del
XM_017028806.1:c.*445_*516del	XP_016884295.1:n.*445_*516del
NM_002473.6:c.*445_*516del MANE Select	NP_002464.1:n.*445_*516del