Canonical Allele Identifier: CA2624230982
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419716_23419723del , CM000676.2:g.23419716_23419723del GRCh38
NC_000014.8:g.23888925_23888932del , CM000676.1:g.23888925_23888932del GRCh37
NC_000014.7:g.22958765_22958772del NCBI36
NG_007884.1:g.20940_20947del , LRG_384:g.20940_20947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3727-113_3727-106del MANE Select ENSP00000347507.3:n.3727-113_3727-106del
ENST00000355349.3:c.3727-113_3727-106del ENSP00000347507.3:n.3727-113_3727-106del
NM_000257.3:c.3727-113_3727-106del NP_000248.2:n.3727-113_3727-106del
XM_017021340.1:c.3727-113_3727-106del XP_016876829.1:n.3727-113_3727-106del
NM_000257.4:c.3727-113_3727-106del MANE Select NP_000248.2:n.3727-113_3727-106del