Canonical Allele Identifier: CA2624251265
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431559del , CM000676.2:g.23431559del GRCh38
NC_000014.8:g.23900768del , CM000676.1:g.23900768del GRCh37
NC_000014.7:g.22970608del NCBI36
NG_007884.1:g.9105del , LRG_384:g.9105del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.732+28del MANE Select ENSP00000347507.3:n.732+28del
ENST00000355349.3:c.732+28del ENSP00000347507.3:n.732+28del
NM_000257.3:c.732+28del NP_000248.2:n.732+28del
XR_245686.3:n.838+28del
XM_017021340.1:c.732+28del XP_016876829.1:n.732+28del
NM_000257.4:c.732+28del MANE Select NP_000248.2:n.732+28del