Canonical Allele Identifier: CA2624230046

Gene: MYH7

Linked Data

• gnomAD v4: 14-23419378-CTCTGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419386_23419391del , CM000676.2:g.23419386_23419391del	GRCh38
NC_000014.8:g.23888595_23888600del , CM000676.1:g.23888595_23888600del	GRCh37
NC_000014.7:g.22958435_22958440del	NCBI36
NG_007884.1:g.21278_21283del , LRG_384:g.21278_21283del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3854-89_3854-84del MANE Select	ENSP00000347507.3:n.3854-89_3854-84del
ENST00000355349.3:c.3854-89_3854-84del	ENSP00000347507.3:n.3854-89_3854-84del
NM_000257.3:c.3854-89_3854-84del	NP_000248.2:n.3854-89_3854-84del
XM_017021340.1:c.3854-89_3854-84del	XP_016876829.1:n.3854-89_3854-84del
NM_000257.4:c.3854-89_3854-84del MANE Select	NP_000248.2:n.3854-89_3854-84del