Canonical Allele Identifier: CA2624235560

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423457-A-ACG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423458_23423459insGC , CM000676.2:g.23423458_23423459insGC	GRCh38
NC_000014.8:g.23892667_23892668insGC , CM000676.1:g.23892667_23892668insGC	GRCh37
NC_000014.7:g.22962507_22962508insGC	NCBI36
NG_007884.1:g.17204_17205insCG , LRG_384:g.17204_17205insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+89_3099+90insCG MANE Select	ENSP00000347507.3:n.3099+89_3099+90insCG
ENST00000355349.3:c.3099+89_3099+90insCG	ENSP00000347507.3:n.3099+89_3099+90insCG
NM_000257.3:c.3099+89_3099+90insCG	NP_000248.2:n.3099+89_3099+90insCG
XR_245686.3:n.3205+89_3205+90insCG
XM_017021340.1:c.3099+89_3099+90insCG	XP_016876829.1:n.3099+89_3099+90insCG
NM_000257.4:c.3099+89_3099+90insCG MANE Select	NP_000248.2:n.3099+89_3099+90insCG