Canonical Allele Identifier: CA2123464599

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415811_23415812delinsCG , CM000676.2:g.23415811_23415812delinsCG GRCh38
NC_000014.8:g.23885020_23885021delinsCG , CM000676.1:g.23885020_23885021delinsCG GRCh37
NC_000014.7:g.22954860_22954861delinsCG NCBI36
NG_007884.1:g.24850_24851delinsCG , LRG_384:g.24850_24851delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4974_4975delinsCG (MYH7) MANE Select ENSP00000347507.3:p.Asp1658=
ENST00000355349.3:c.4974_4975delinsCG (MYH7) ENSP00000347507.3:p.Asp1658=
NM_000257.3:c.4974_4975delinsCG (MYH7) NP_000248.2:p.Asp1658=
NR_126491.1:n.243_244delinsCG (MHRT)
XM_017021340.1:c.4974_4975delinsCG (MYH7) XP_016876829.1:p.Asp1658=
NM_000257.4:c.4974_4975delinsCG (MYH7) MANE Select NP_000248.2:p.Asp1658=