Canonical Allele Identifier: CA2656426781
Gene: MYH9 HGNC NCBI

Linked Data

gnomAD v4: 22-36282284-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36282288del , CM000684.2:g.36282288del GRCh38
NC_000022.10:g.36678334del , CM000684.1:g.36678334del GRCh37
NC_000022.9:g.35008280del NCBI36
NG_011884.2:g.110734del , LRG_567:g.110734del

Transcript Alleles

HGVS Amino-acid Change
ENST00000685708.1:n.2699del
ENST00000685801.1:c.*383del ENSP00000510688.1:n.*383del
ENST00000690244.1:n.1602del
ENST00000691109.1:n.6561del
ENST00000216181.11:c.*383del MANE Select ENSP00000216181.6:n.*383del
ENST00000216181.9:c.*383del ENSP00000216181.5:n.*383del
NM_002473.5:c.*383del , LRG_567t1:c.*383del NP_002464.1:n.*383del
XM_011530197.1:c.*383del XP_011528499.1:n.*383del
XM_011530197.2:c.*383del XP_011528499.1:n.*383del
XM_017028803.1:c.*383del XP_016884292.1:n.*383del
XM_017028804.1:c.*383del XP_016884293.1:n.*383del
XM_017028805.1:c.*383del XP_016884294.1:n.*383del
XM_017028806.1:c.*383del XP_016884295.1:n.*383del
NM_002473.6:c.*383del MANE Select NP_002464.1:n.*383del
Search 100 bp 5'
Search 100 bp 3'