Canonical Allele Identifier: CA2800863558

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419466_23419467insT , CM000676.2:g.23419466_23419467insT	GRCh38
NC_000014.8:g.23888675_23888676insT , CM000676.1:g.23888675_23888676insT	GRCh37
NC_000014.7:g.22958515_22958516insT	NCBI36
NG_007884.1:g.21195_21196insA , LRG_384:g.21195_21196insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3853+16_3853+17insA MANE Select	ENSP00000347507.3:n.3853+16_3853+17insA
ENST00000355349.3:c.3853+16_3853+17insA	ENSP00000347507.3:n.3853+16_3853+17insA
NM_000257.3:c.3853+16_3853+17insA	NP_000248.2:n.3853+16_3853+17insA
XM_017021340.1:c.3853+16_3853+17insA	XP_016876829.1:n.3853+16_3853+17insA
NM_000257.4:c.3853+16_3853+17insA MANE Select	NP_000248.2:n.3853+16_3853+17insA