Canonical Allele Identifier: CA2624235074

Gene: MYH7 MHRT

Linked Data

• gnomAD v4: 14-23416359-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23416362del , CM000676.2:g.23416362del	GRCh38
NC_000014.8:g.23885571del , CM000676.1:g.23885571del	GRCh37
NC_000014.7:g.22955411del	NCBI36
NG_007884.1:g.24302del , LRG_384:g.24302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4645-48del (MYH7) MANE Select	ENSP00000347507.3:n.4645-48del
ENST00000355349.3:c.4645-48del (MYH7)	ENSP00000347507.3:n.4645-48del
NM_000257.3:c.4645-48del (MYH7)	NP_000248.2:n.4645-48del
NR_126491.1:n.558+65del (MHRT)
XM_017021340.1:c.4645-48del (MYH7)	XP_016876829.1:n.4645-48del
NM_000257.4:c.4645-48del (MYH7) MANE Select	NP_000248.2:n.4645-48del