Canonical Allele Identifier: CA2624235580

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423469-A-AGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423469_23423470insGAG , CM000676.2:g.23423469_23423470insGAG	GRCh38
NC_000014.8:g.23892678_23892679insGAG , CM000676.1:g.23892678_23892679insGAG	GRCh37
NC_000014.7:g.22962518_22962519insGAG	NCBI36
NG_007884.1:g.17192_17193insCTC , LRG_384:g.17192_17193insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+77_3099+78insCTC MANE Select	ENSP00000347507.3:n.3099+77_3099+78insCTC
ENST00000355349.3:c.3099+77_3099+78insCTC	ENSP00000347507.3:n.3099+77_3099+78insCTC
NM_000257.3:c.3099+77_3099+78insCTC	NP_000248.2:n.3099+77_3099+78insCTC
XR_245686.3:n.3205+77_3205+78insCTC
XM_017021340.1:c.3099+77_3099+78insCTC	XP_016876829.1:n.3099+77_3099+78insCTC
NM_000257.4:c.3099+77_3099+78insCTC MANE Select	NP_000248.2:n.3099+77_3099+78insCTC