Canonical Allele Identifier: CA2624237812

Gene: MYH7 MHRT

Linked Data

• gnomAD v4: 14-23417469-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417470del , CM000676.2:g.23417470del	GRCh38
NC_000014.8:g.23886679del , CM000676.1:g.23886679del	GRCh37
NC_000014.7:g.22956519del	NCBI36
NG_007884.1:g.23192del , LRG_384:g.23192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4353+33del (MYH7) MANE Select	ENSP00000347507.3:n.4353+33del
ENST00000355349.3:c.4353+33del (MYH7)	ENSP00000347507.3:n.4353+33del
NM_000257.3:c.4353+33del (MYH7)	NP_000248.2:n.4353+33del
NR_126491.1:n.814-63del (MHRT)
XM_017021340.1:c.4353+33del (MYH7)	XP_016876829.1:n.4353+33del
NM_000257.4:c.4353+33del (MYH7) MANE Select	NP_000248.2:n.4353+33del