Canonical Allele Identifier: CA2624236921
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423895_23423898dup , CM000676.2:g.23423895_23423898dup GRCh38
NC_000014.8:g.23893104_23893107dup , CM000676.1:g.23893104_23893107dup GRCh37
NC_000014.7:g.22962944_22962947dup NCBI36
NG_007884.1:g.16764_16767dup , LRG_384:g.16764_16767dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2922+9_2922+12dup MANE Select ENSP00000347507.3:n.2922+9_2922+12dup
ENST00000355349.3:c.2922+9_2922+12dup ENSP00000347507.3:n.2922+9_2922+12dup
NM_000257.3:c.2922+9_2922+12dup NP_000248.2:n.2922+9_2922+12dup
XR_245686.3:n.3028+9_3028+12dup
XM_017021340.1:c.2922+9_2922+12dup XP_016876829.1:n.2922+9_2922+12dup
NM_000257.4:c.2922+9_2922+12dup MANE Select NP_000248.2:n.2922+9_2922+12dup