Canonical Allele Identifier: CA323584759
Gene: MYH9 HGNC NCBI

Linked Data

dbSNP Id: rs35347691

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36281982del , CM000684.2:g.36281982del GRCh38
NC_000022.10:g.36678028del , CM000684.1:g.36678028del GRCh37
NC_000022.9:g.35007974del NCBI36
NG_011884.2:g.111040del , LRG_567:g.111040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000685708.1:n.3005del
ENST00000685801.1:c.*689del ENSP00000510688.1:n.*689del
ENST00000690244.1:n.1908del
ENST00000691109.1:n.6867del
ENST00000216181.11:c.*689del MANE Select ENSP00000216181.6:n.*689del
ENST00000216181.9:c.*689del ENSP00000216181.5:n.*689del
NM_002473.5:c.*689del , LRG_567t1:c.*689del NP_002464.1:n.*689del
XM_011530197.1:c.*689del XP_011528499.1:n.*689del
XM_011530197.2:c.*689del XP_011528499.1:n.*689del
XM_017028803.1:c.*689del XP_016884292.1:n.*689del
XM_017028804.1:c.*689del XP_016884293.1:n.*689del
XM_017028805.1:c.*689del XP_016884294.1:n.*689del
XM_017028806.1:c.*689del XP_016884295.1:n.*689del
NM_002473.6:c.*689del MANE Select NP_002464.1:n.*689del