Canonical Allele Identifier: CA2123445779

Gene: MYH7

Linked Data

• dbSNP Id: rs1892389716

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419721_23419727del , CM000676.2:g.23419721_23419727del	GRCh38
NC_000014.8:g.23888930_23888936del , CM000676.1:g.23888930_23888936del	GRCh37
NC_000014.7:g.22958770_22958776del	NCBI36
NG_007884.1:g.20936_20942del , LRG_384:g.20936_20942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-117_3727-111del MANE Select	ENSP00000347507.3:n.3727-117_3727-111del
ENST00000355349.3:c.3727-117_3727-111del	ENSP00000347507.3:n.3727-117_3727-111del
NM_000257.3:c.3727-117_3727-111del	NP_000248.2:n.3727-117_3727-111del
XM_017021340.1:c.3727-117_3727-111del	XP_016876829.1:n.3727-117_3727-111del
NM_000257.4:c.3727-117_3727-111del MANE Select	NP_000248.2:n.3727-117_3727-111del