Canonical Allele Identifier: CA2624230093

Gene: MYH7

Linked Data

• gnomAD v4: 14-23419405-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419407dup , CM000676.2:g.23419407dup	GRCh38
NC_000014.8:g.23888616dup , CM000676.1:g.23888616dup	GRCh37
NC_000014.7:g.22958456dup	NCBI36
NG_007884.1:g.21256dup , LRG_384:g.21256dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3853+77dup MANE Select	ENSP00000347507.3:n.3853+77dup
ENST00000355349.3:c.3853+77dup	ENSP00000347507.3:n.3853+77dup
NM_000257.3:c.3853+77dup	NP_000248.2:n.3853+77dup
XM_017021340.1:c.3853+77dup	XP_016876829.1:n.3853+77dup
NM_000257.4:c.3853+77dup MANE Select	NP_000248.2:n.3853+77dup