Canonical Allele Identifier: CA2123469111

Gene: MYH7 MHRT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417482_23417483delinsCG , CM000676.2:g.23417482_23417483delinsCG	GRCh38
NC_000014.8:g.23886691_23886692delinsCG , CM000676.1:g.23886691_23886692delinsCG	GRCh37
NC_000014.7:g.22956531_22956532delinsCG	NCBI36
NG_007884.1:g.23179_23180delinsCG , LRG_384:g.23179_23180delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4353+20_4353+21delinsCG (MYH7) MANE Select	ENSP00000347507.3:n.4353+20_4353+21delinsCG
ENST00000355349.3:c.4353+20_4353+21delinsCG (MYH7)	ENSP00000347507.3:n.4353+20_4353+21delinsCG
NM_000257.3:c.4353+20_4353+21delinsCG (MYH7)	NP_000248.2:n.4353+20_4353+21delinsCG
NR_126491.1:n.814-51_814-50delinsCG (MHRT)
XM_017021340.1:c.4353+20_4353+21delinsCG (MYH7)	XP_016876829.1:n.4353+20_4353+21delinsCG
NM_000257.4:c.4353+20_4353+21delinsCG (MYH7) MANE Select	NP_000248.2:n.4353+20_4353+21delinsCG