Canonical Allele Identifier: CA2624233704

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415860_23415866del , CM000676.2:g.23415860_23415866del GRCh38
NC_000014.8:g.23885069_23885075del , CM000676.1:g.23885069_23885075del GRCh37
NC_000014.7:g.22954909_22954915del NCBI36
NG_007884.1:g.24800_24806del , LRG_384:g.24800_24806del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4954-30_4954-24del (MYH7) MANE Select ENSP00000347507.3:n.4954-30_4954-24del
ENST00000355349.3:c.4954-30_4954-24del (MYH7) ENSP00000347507.3:n.4954-30_4954-24del
NM_000257.3:c.4954-30_4954-24del (MYH7) NP_000248.2:n.4954-30_4954-24del
NR_126491.1:n.261+31_261+37del (MHRT)
XM_017021340.1:c.4954-30_4954-24del (MYH7) XP_016876829.1:n.4954-30_4954-24del
NM_000257.4:c.4954-30_4954-24del (MYH7) MANE Select NP_000248.2:n.4954-30_4954-24del