Canonical Allele Identifier: CA2123455238
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424489_23424490delinsAG , CM000676.2:g.23424489_23424490delinsAG GRCh38
NC_000014.8:g.23893698_23893699delinsAG , CM000676.1:g.23893698_23893699delinsAG GRCh37
NC_000014.7:g.22963538_22963539delinsAG NCBI36
NG_007884.1:g.16172_16173delinsCT , LRG_384:g.16172_16173delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2679+279_2679+280delinsCT MANE Select ENSP00000347507.3:n.2679+279_2679+280delinsCT
ENST00000355349.3:c.2679+279_2679+280delinsCT ENSP00000347507.3:n.2679+279_2679+280delinsCT
NM_000257.3:c.2679+279_2679+280delinsCT NP_000248.2:n.2679+279_2679+280delinsCT
XR_245686.3:n.2785+279_2785+280delinsCT
XM_017021340.1:c.2679+279_2679+280delinsCT XP_016876829.1:n.2679+279_2679+280delinsCT
NM_000257.4:c.2679+279_2679+280delinsCT MANE Select NP_000248.2:n.2679+279_2679+280delinsCT