Canonical Allele Identifier: CA2800863602

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419686_23419690del , CM000676.2:g.23419686_23419690del	GRCh38
NC_000014.8:g.23888895_23888899del , CM000676.1:g.23888895_23888899del	GRCh37
NC_000014.7:g.22958735_22958739del	NCBI36
NG_007884.1:g.20972_20976del , LRG_384:g.20972_20976del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-81_3727-77del MANE Select	ENSP00000347507.3:n.3727-81_3727-77del
ENST00000355349.3:c.3727-81_3727-77del	ENSP00000347507.3:n.3727-81_3727-77del
NM_000257.3:c.3727-81_3727-77del	NP_000248.2:n.3727-81_3727-77del
XM_017021340.1:c.3727-81_3727-77del	XP_016876829.1:n.3727-81_3727-77del
NM_000257.4:c.3727-81_3727-77del MANE Select	NP_000248.2:n.3727-81_3727-77del