Canonical Allele Identifier: CA2624234047

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416021_23416022del , CM000676.2:g.23416021_23416022del GRCh38
NC_000014.8:g.23885230_23885231del , CM000676.1:g.23885230_23885231del GRCh37
NC_000014.7:g.22955070_22955071del NCBI36
NG_007884.1:g.24640_24641del , LRG_384:g.24640_24641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4935_4936del (MYH7) MANE Select ENSP00000347507.3:p.Leu1646ProfsTer?
ENST00000355349.3:c.4935_4936del (MYH7) ENSP00000347507.3:p.Leu1646ProfsTer?
NM_000257.3:c.4935_4936del (MYH7) NP_000248.2:p.Leu1646ProfsTer?
NR_126491.1:n.282_283del (MHRT)
XM_017021340.1:c.4935_4936del (MYH7) XP_016876829.1:p.Leu1646ProfsTer?
NM_000257.4:c.4935_4936del (MYH7) MANE Select NP_000248.2:p.Leu1646ProfsTer?