Canonical Allele Identifier: CA2123457829

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425460_23425468delinsCGAGGGAAA , CM000676.2:g.23425460_23425468delinsCGAGGGAAA	GRCh38
NC_000014.8:g.23894669_23894677delinsCGAGGGAAA , CM000676.1:g.23894669_23894677delinsCGAGGGAAA	GRCh37
NC_000014.7:g.22964509_22964517delinsCGAGGGAAA	NCBI36
NG_007884.1:g.15194_15202delinsTTTCCCTCG , LRG_384:g.15194_15202delinsTTTCCCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2287-50_2287-42delinsTTTCCCTCG MANE Select	ENSP00000347507.3:n.2287-50_2287-42delinsTTTCCCTCG
ENST00000355349.3:c.2287-50_2287-42delinsTTTCCCTCG	ENSP00000347507.3:n.2287-50_2287-42delinsTTTCCCTCG
NM_000257.3:c.2287-50_2287-42delinsTTTCCCTCG	NP_000248.2:n.2287-50_2287-42delinsTTTCCCTCG
XR_245686.3:n.2393-50_2393-42delinsTTTCCCTCG
XM_017021340.1:c.2287-50_2287-42delinsTTTCCCTCG	XP_016876829.1:n.2287-50_2287-42delinsTTTCCCTCG
NM_000257.4:c.2287-50_2287-42delinsTTTCCCTCG MANE Select	NP_000248.2:n.2287-50_2287-42delinsTTTCCCTCG