Canonical Allele Identifier: CA2123447550

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420322_23420323delinsAC , CM000676.2:g.23420322_23420323delinsAC	GRCh38
NC_000014.8:g.23889531_23889532delinsAC , CM000676.1:g.23889531_23889532delinsAC	GRCh37
NC_000014.7:g.22959371_22959372delinsAC	NCBI36
NG_007884.1:g.20339_20340delinsGT , LRG_384:g.20339_20340delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-89_3337-88delinsGT MANE Select	ENSP00000347507.3:n.3337-89_3337-88delinsGT
ENST00000355349.3:c.3337-89_3337-88delinsGT	ENSP00000347507.3:n.3337-89_3337-88delinsGT
NM_000257.3:c.3337-89_3337-88delinsGT	NP_000248.2:n.3337-89_3337-88delinsGT
XR_245686.3:n.3445-89_3445-88delinsGT
XM_017021340.1:c.3337-89_3337-88delinsGT	XP_016876829.1:n.3337-89_3337-88delinsGT
NM_000257.4:c.3337-89_3337-88delinsGT MANE Select	NP_000248.2:n.3337-89_3337-88delinsGT