Canonical Allele Identifier: CA2800863408

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423438_23423439insCT , CM000676.2:g.23423438_23423439insCT	GRCh38
NC_000014.8:g.23892647_23892648insCT , CM000676.1:g.23892647_23892648insCT	GRCh37
NC_000014.7:g.22962487_22962488insCT	NCBI36
NG_007884.1:g.17223_17224insAG , LRG_384:g.17223_17224insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+108_3099+109insAG MANE Select	ENSP00000347507.3:n.3099+108_3099+109insAG
ENST00000355349.3:c.3099+108_3099+109insAG	ENSP00000347507.3:n.3099+108_3099+109insAG
NM_000257.3:c.3099+108_3099+109insAG	NP_000248.2:n.3099+108_3099+109insAG
XR_245686.3:n.3205+108_3205+109insAG
XM_017021340.1:c.3099+108_3099+109insAG	XP_016876829.1:n.3099+108_3099+109insAG
NM_000257.4:c.3099+108_3099+109insAG MANE Select	NP_000248.2:n.3099+108_3099+109insAG