Canonical Allele Identifier: CA2624239156

Gene: MYH7

Linked Data

• gnomAD v4: 14-23417862-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417865_23417866dup , CM000676.2:g.23417865_23417866dup	GRCh38
NC_000014.8:g.23887074_23887075dup , CM000676.1:g.23887074_23887075dup	GRCh37
NC_000014.7:g.22956914_22956915dup	NCBI36
NG_007884.1:g.22798_22799dup , LRG_384:g.22798_22799dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-178_4170-177dup MANE Select	ENSP00000347507.3:n.4170-178_4170-177dup
ENST00000355349.3:c.4170-178_4170-177dup	ENSP00000347507.3:n.4170-178_4170-177dup
NM_000257.3:c.4170-178_4170-177dup	NP_000248.2:n.4170-178_4170-177dup
XM_017021340.1:c.4170-178_4170-177dup	XP_016876829.1:n.4170-178_4170-177dup
NM_000257.4:c.4170-178_4170-177dup MANE Select	NP_000248.2:n.4170-178_4170-177dup