Canonical Allele Identifier: CA2624229612

Gene: MYH7

Linked Data

• gnomAD v4: 14-23425456-G-GCCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425456_23425457insCCAT , CM000676.2:g.23425456_23425457insCCAT	GRCh38
NC_000014.8:g.23894665_23894666insCCAT , CM000676.1:g.23894665_23894666insCCAT	GRCh37
NC_000014.7:g.22964505_22964506insCCAT	NCBI36
NG_007884.1:g.15205_15206insATGG , LRG_384:g.15205_15206insATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2287-39_2287-38insATGG MANE Select	ENSP00000347507.3:n.2287-39_2287-38insATGG
ENST00000355349.3:c.2287-39_2287-38insATGG	ENSP00000347507.3:n.2287-39_2287-38insATGG
NM_000257.3:c.2287-39_2287-38insATGG	NP_000248.2:n.2287-39_2287-38insATGG
XR_245686.3:n.2393-39_2393-38insATGG
XM_017021340.1:c.2287-39_2287-38insATGG	XP_016876829.1:n.2287-39_2287-38insATGG
NM_000257.4:c.2287-39_2287-38insATGG MANE Select	NP_000248.2:n.2287-39_2287-38insATGG