Canonical Allele Identifier: CA2741360396

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420294dup , CM000676.2:g.23420294dup	GRCh38
NC_000014.8:g.23889503dup , CM000676.1:g.23889503dup	GRCh37
NC_000014.7:g.22959343dup	NCBI36
NG_007884.1:g.20369dup , LRG_384:g.20369dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-59dup MANE Select	ENSP00000347507.3:n.3337-59dup
ENST00000355349.3:c.3337-59dup	ENSP00000347507.3:n.3337-59dup
NM_000257.3:c.3337-59dup	NP_000248.2:n.3337-59dup
XR_245686.3:n.3445-59dup
XM_017021340.1:c.3337-59dup	XP_016876829.1:n.3337-59dup
NM_000257.4:c.3337-59dup MANE Select	NP_000248.2:n.3337-59dup