Canonical Allele Identifier: CA2568410877

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423440_23423441insGC , CM000676.2:g.23423440_23423441insGC	GRCh38
NC_000014.8:g.23892649_23892650insGC , CM000676.1:g.23892649_23892650insGC	GRCh37
NC_000014.7:g.22962489_22962490insGC	NCBI36
NG_007884.1:g.17222_17223insCG , LRG_384:g.17222_17223insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+107_3099+108insCG MANE Select	ENSP00000347507.3:n.3099+107_3099+108insCG
ENST00000355349.3:c.3099+107_3099+108insCG	ENSP00000347507.3:n.3099+107_3099+108insCG
NM_000257.3:c.3099+107_3099+108insCG	NP_000248.2:n.3099+107_3099+108insCG
XR_245686.3:n.3205+107_3205+108insCG
XM_017021340.1:c.3099+107_3099+108insCG	XP_016876829.1:n.3099+107_3099+108insCG
NM_000257.4:c.3099+107_3099+108insCG MANE Select	NP_000248.2:n.3099+107_3099+108insCG