Canonical Allele Identifier: CA2624237904

Gene: MYH7 MHRT

Linked Data

• gnomAD v4: 14-23417478-GCTGCGGCCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417480_23417489del , CM000676.2:g.23417480_23417489del	GRCh38
NC_000014.8:g.23886689_23886698del , CM000676.1:g.23886689_23886698del	GRCh37
NC_000014.7:g.22956529_22956538del	NCBI36
NG_007884.1:g.23174_23183del , LRG_384:g.23174_23183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4353+15_4353+24del (MYH7) MANE Select	ENSP00000347507.3:n.4353+15_4353+24del
ENST00000355349.3:c.4353+15_4353+24del (MYH7)	ENSP00000347507.3:n.4353+15_4353+24del
NM_000257.3:c.4353+15_4353+24del (MYH7)	NP_000248.2:n.4353+15_4353+24del
NR_126491.1:n.814-53_814-44del (MHRT)
XM_017021340.1:c.4353+15_4353+24del (MYH7)	XP_016876829.1:n.4353+15_4353+24del
NM_000257.4:c.4353+15_4353+24del (MYH7) MANE Select	NP_000248.2:n.4353+15_4353+24del