Canonical Allele Identifier: CA2624233959
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422055dup , CM000676.2:g.23422055dup GRCh38
NC_000014.8:g.23891264dup , CM000676.1:g.23891264dup GRCh37
NC_000014.7:g.22961104dup NCBI36
NG_007884.1:g.18609dup , LRG_384:g.18609dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+127dup MANE Select ENSP00000347507.3:n.3245+127dup
ENST00000355349.3:c.3245+127dup ENSP00000347507.3:n.3245+127dup
NM_000257.3:c.3245+127dup NP_000248.2:n.3245+127dup
XR_245686.3:n.3351+127dup
XM_017021340.1:c.3245+127dup XP_016876829.1:n.3245+127dup
NM_000257.4:c.3245+127dup MANE Select NP_000248.2:n.3245+127dup