Canonical Allele Identifier: CA2123469090

Gene: MYH7 MHRT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417479_23417480delinsCT , CM000676.2:g.23417479_23417480delinsCT	GRCh38
NC_000014.8:g.23886688_23886689delinsCT , CM000676.1:g.23886688_23886689delinsCT	GRCh37
NC_000014.7:g.22956528_22956529delinsCT	NCBI36
NG_007884.1:g.23182_23183delinsAG , LRG_384:g.23182_23183delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4353+23_4353+24delinsAG (MYH7) MANE Select	ENSP00000347507.3:n.4353+23_4353+24delinsAG
ENST00000355349.3:c.4353+23_4353+24delinsAG (MYH7)	ENSP00000347507.3:n.4353+23_4353+24delinsAG
NM_000257.3:c.4353+23_4353+24delinsAG (MYH7)	NP_000248.2:n.4353+23_4353+24delinsAG
NR_126491.1:n.814-54_814-53delinsCT (MHRT)
XM_017021340.1:c.4353+23_4353+24delinsAG (MYH7)	XP_016876829.1:n.4353+23_4353+24delinsAG
NM_000257.4:c.4353+23_4353+24delinsAG (MYH7) MANE Select	NP_000248.2:n.4353+23_4353+24delinsAG