Canonical Allele Identifier: CA2123464604

Linked Data

dbSNP Id: rs1892177529

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415812del , CM000676.2:g.23415812del GRCh38
NC_000014.8:g.23885021del , CM000676.1:g.23885021del GRCh37
NC_000014.7:g.22954861del NCBI36
NG_007884.1:g.24850del , LRG_384:g.24850del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4974del (MYH7) MANE Select ENSP00000347507.3:p.Asp1658GlufsTer10
ENST00000355349.3:c.4974del (MYH7) ENSP00000347507.3:p.Asp1658GlufsTer10
NM_000257.3:c.4974del (MYH7) NP_000248.2:p.Asp1658GlufsTer10
NR_126491.1:n.244del (MHRT)
XM_017021340.1:c.4974del (MYH7) XP_016876829.1:p.Asp1658GlufsTer10
NM_000257.4:c.4974del (MYH7) MANE Select NP_000248.2:p.Asp1658GlufsTer10