Canonical Allele Identifier: CA2842879861

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420936del , CM000676.2:g.23420936del	GRCh38
NC_000014.8:g.23890145del , CM000676.1:g.23890145del	GRCh37
NC_000014.7:g.22959985del	NCBI36
NG_007884.1:g.19728del , LRG_384:g.19728del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+24del MANE Select	ENSP00000347507.3:n.3336+24del
ENST00000355349.3:c.3336+24del	ENSP00000347507.3:n.3336+24del
NM_000257.3:c.3336+24del	NP_000248.2:n.3336+24del
XR_245686.3:n.3444+24del
XM_017021340.1:c.3336+24del	XP_016876829.1:n.3336+24del
NM_000257.4:c.3336+24del MANE Select	NP_000248.2:n.3336+24del