Canonical Allele Identifier: CA2624250384

Gene: MYH7

Linked Data

• gnomAD v4: 14-23430816-G-GCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23430816_23430817insCTC , CM000676.2:g.23430816_23430817insCTC	GRCh38
NC_000014.8:g.23900025_23900026insCTC , CM000676.1:g.23900025_23900026insCTC	GRCh37
NC_000014.7:g.22969865_22969866insCTC	NCBI36
NG_007884.1:g.9845_9846insGAG , LRG_384:g.9845_9846insGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.895+84_895+85insGAG MANE Select	ENSP00000347507.3:n.895+84_895+85insGAG
ENST00000355349.3:c.895+84_895+85insGAG	ENSP00000347507.3:n.895+84_895+85insGAG
NM_000257.3:c.895+84_895+85insGAG	NP_000248.2:n.895+84_895+85insGAG
XR_245686.3:n.1001+84_1001+85insGAG
XM_017021340.1:c.895+84_895+85insGAG	XP_016876829.1:n.895+84_895+85insGAG
NM_000257.4:c.895+84_895+85insGAG MANE Select	NP_000248.2:n.895+84_895+85insGAG