Canonical Allele Identifier: CA2624238841
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417771_23417780del , CM000676.2:g.23417771_23417780del GRCh38
NC_000014.8:g.23886980_23886989del , CM000676.1:g.23886980_23886989del GRCh37
NC_000014.7:g.22956820_22956829del NCBI36
NG_007884.1:g.22884_22893del , LRG_384:g.22884_22893del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-92_4170-83del MANE Select ENSP00000347507.3:n.4170-92_4170-83del
ENST00000355349.3:c.4170-92_4170-83del ENSP00000347507.3:n.4170-92_4170-83del
NM_000257.3:c.4170-92_4170-83del NP_000248.2:n.4170-92_4170-83del
XM_017021340.1:c.4170-92_4170-83del XP_016876829.1:n.4170-92_4170-83del
NM_000257.4:c.4170-92_4170-83del MANE Select NP_000248.2:n.4170-92_4170-83del