Canonical Allele Identifier: CA2652580946
Gene: MYH7B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34977944_34977954del , CM000682.2:g.34977944_34977954del GRCh38
NC_000020.10:g.33565747_33565757del , CM000682.1:g.33565747_33565757del GRCh37
NC_000020.9:g.33029408_33029418del NCBI36
NG_016984.2:g.27044_27054del

Transcript Alleles

HGVS Amino-acid change
ENST00000262873.13:c.-62_-52del MANE Select ENSP00000262873.8:n.-62_-52del
ENST00000262873.12:c.-62_-52del ENSP00000262873.8:n.-62_-52del
ENST00000618182.6:c.62_72del ENSP00000483640.3:p.Pro21LeufsTer23
ENST00000673749.1:n.473_483del
ENST00000262873.11:c.65_75del ENSP00000262873.7:p.Pro22LeufsTer23
ENST00000470929.5:n.25_35del
ENST00000618182.4:c.62_72del ENSP00000483640.1:p.Pro21LeufsTer23
NM_020884.4:c.65_75del NP_065935.3:p.Pro22LeufsTer23
XM_006723840.2:c.65_75del XP_006723903.1:p.Pro22LeufsTer23
XM_011528941.1:c.65_75del XP_011527243.1:p.Pro22LeufsTer23
XM_011528942.1:c.65_75del XP_011527244.1:p.Pro22LeufsTer23
XM_011528943.1:c.65_75del XP_011527245.1:p.Pro22LeufsTer23
XM_011528944.1:c.65_75del XP_011527246.1:p.Pro22LeufsTer23
XM_011528945.1:c.-445_-435del XP_011527247.1:n.-445_-435del
XM_011528950.1:c.65_75del XP_011527252.1:p.Pro22LeufsTer23
XM_006723840.3:c.65_75del XP_006723903.1:p.Pro22LeufsTer23
XM_011528941.2:c.65_75del XP_011527243.1:p.Pro22LeufsTer23
XM_017027986.1:c.65_75del XP_016883475.1:p.Pro22LeufsTer23
NM_020884.5:c.65_75del NP_065935.3:p.Pro22LeufsTer23
NM_020884.7:c.-62_-52del MANE Select NP_065935.4:n.-62_-52del