Canonical Allele Identifier: CA2403794937
Gene: MYH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36281983_36281984delinsAG , CM000684.2:g.36281983_36281984delinsAG GRCh38
NC_000022.10:g.36678029_36678030delinsAG , CM000684.1:g.36678029_36678030delinsAG GRCh37
NC_000022.9:g.35007975_35007976delinsAG NCBI36
NG_011884.2:g.111035_111036delinsCT , LRG_567:g.111035_111036delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000685708.1:n.3000_3001delinsCT
ENST00000685801.1:c.*684_*685delinsCT ENSP00000510688.1:n.*684_*685delinsCT
ENST00000690244.1:n.1903_1904delinsCT
ENST00000691109.1:n.6862_6863delinsCT
ENST00000216181.11:c.*684_*685delinsCT MANE Select ENSP00000216181.6:n.*684_*685delinsCT
ENST00000216181.9:c.*684_*685delinsCT ENSP00000216181.5:n.*684_*685delinsCT
NM_002473.5:c.*684_*685delinsCT , LRG_567t1:c.*684_*685delinsCT NP_002464.1:n.*684_*685delinsCT
XM_011530197.1:c.*684_*685delinsCT XP_011528499.1:n.*684_*685delinsCT
XM_011530197.2:c.*684_*685delinsCT XP_011528499.1:n.*684_*685delinsCT
XM_017028803.1:c.*684_*685delinsCT XP_016884292.1:n.*684_*685delinsCT
XM_017028804.1:c.*684_*685delinsCT XP_016884293.1:n.*684_*685delinsCT
XM_017028805.1:c.*684_*685delinsCT XP_016884294.1:n.*684_*685delinsCT
XM_017028806.1:c.*684_*685delinsCT XP_016884295.1:n.*684_*685delinsCT
NM_002473.6:c.*684_*685delinsCT MANE Select NP_002464.1:n.*684_*685delinsCT