Canonical Allele Identifier: CA2842814670

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23424175dup , CM000676.2:g.23424175dup	GRCh38
NC_000014.8:g.23893384dup , CM000676.1:g.23893384dup	GRCh37
NC_000014.7:g.22963224dup	NCBI36
NG_007884.1:g.16487dup , LRG_384:g.16487dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2680-26dup MANE Select	ENSP00000347507.3:n.2680-26dup
ENST00000355349.3:c.2680-26dup	ENSP00000347507.3:n.2680-26dup
NM_000257.3:c.2680-26dup	NP_000248.2:n.2680-26dup
XR_245686.3:n.2786-26dup
XM_017021340.1:c.2680-26dup	XP_016876829.1:n.2680-26dup
NM_000257.4:c.2680-26dup MANE Select	NP_000248.2:n.2680-26dup