Canonical Allele Identifier: CA2624235091

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423419-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423420del , CM000676.2:g.23423420del	GRCh38
NC_000014.8:g.23892629del , CM000676.1:g.23892629del	GRCh37
NC_000014.7:g.22962469del	NCBI36
NG_007884.1:g.17242del , LRG_384:g.17242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+127del MANE Select	ENSP00000347507.3:n.3099+127del
ENST00000355349.3:c.3099+127del	ENSP00000347507.3:n.3099+127del
NM_000257.3:c.3099+127del	NP_000248.2:n.3099+127del
XR_245686.3:n.3205+127del
XM_017021340.1:c.3099+127del	XP_016876829.1:n.3099+127del
NM_000257.4:c.3099+127del MANE Select	NP_000248.2:n.3099+127del