Canonical Allele Identifier: CA2842879891

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423850dup , CM000676.2:g.23423850dup	GRCh38
NC_000014.8:g.23893059dup , CM000676.1:g.23893059dup	GRCh37
NC_000014.7:g.22962899dup	NCBI36
NG_007884.1:g.16812dup , LRG_384:g.16812dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2922+57dup MANE Select	ENSP00000347507.3:n.2922+57dup
ENST00000355349.3:c.2922+57dup	ENSP00000347507.3:n.2922+57dup
NM_000257.3:c.2922+57dup	NP_000248.2:n.2922+57dup
XR_245686.3:n.3028+57dup
XM_017021340.1:c.2922+57dup	XP_016876829.1:n.2922+57dup
NM_000257.4:c.2922+57dup MANE Select	NP_000248.2:n.2922+57dup