Canonical Allele Identifier: CA389034764

Gene: MYH7

Linked Data

• MyVariant Identifiers: chr14:g.23413922del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23413926del , CM000676.2:g.23413926del	GRCh38
NC_000014.8:g.23883135del , CM000676.1:g.23883135del	GRCh37
NC_000014.7:g.22952975del	NCBI36
NG_007884.1:g.26740del , LRG_384:g.26740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.5656-29del MANE Select	ENSP00000347507.3:n.5656-29del
ENST00000355349.3:c.5656-29del	ENSP00000347507.3:n.5656-29del
NM_000257.3:c.5656-29del	NP_000248.2:n.5656-29del
XM_017021340.1:c.5656-29del	XP_016876829.1:n.5656-29del
NM_000257.4:c.5656-29del MANE Select	NP_000248.2:n.5656-29del