Canonical Allele Identifier: CA3267438993
Community Standard Title: NC_000014.9:g.23431620_23433131dup
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431620_23433131dup , CM000676.2:g.23431620_23433131dup GRCh38
NC_000014.8:g.23900829_23902340dup , CM000676.1:g.23900829_23902340dup GRCh37
NC_000014.7:g.22970669_22972180dup NCBI36
NG_007884.1:g.7531_9042dup , LRG_384:g.7531_9042dup

Transcript Alleles

HGVS Amino-acid Change
NM_000257.3:c.298_697dup
NM_000257.4:c.298_697dup
ENST00000355349.3:c.298_697dup
ENST00000355349.4:c.298_697dup
XM_017021340.1:c.298_697dup
XR_245686.3:n.404_803dup