Canonical Allele Identifier: CA2624234367
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23427583dup , CM000676.2:g.23427583dup GRCh38
NC_000014.8:g.23896792dup , CM000676.1:g.23896792dup GRCh37
NC_000014.7:g.22966632dup NCBI36
NG_007884.1:g.13079dup , LRG_384:g.13079dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1888+2dup MANE Select ENSP00000347507.3:n.1888+2dup
ENST00000355349.3:c.1888+2dup ENSP00000347507.3:n.1888+2dup
NM_000257.3:c.1888+2dup NP_000248.2:n.1888+2dup
XR_245686.3:n.1994+2dup
XM_017021340.1:c.1888+2dup XP_016876829.1:n.1888+2dup
NM_000257.4:c.1888+2dup MANE Select NP_000248.2:n.1888+2dup