Canonical Allele Identifier: CA1139663374

Linked Data

ClinVar Variation Id: 985543
ClinVar RCV Id: RCV001266511
dbSNP Id: rs1892274161

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417571_23417573dup , CM000676.2:g.23417571_23417573dup GRCh38
NC_000014.8:g.23886780_23886782dup , CM000676.1:g.23886780_23886782dup GRCh37
NC_000014.7:g.22956620_22956622dup NCBI36
NG_007884.1:g.23091_23093dup , LRG_384:g.23091_23093dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4285_4287dup (MYH7) MANE Select ENSP00000347507.3:p.Met1429_Val1430insMet
ENST00000355349.3:c.4285_4287dup (MYH7) ENSP00000347507.3:p.Met1429_Val1430insMet
NM_000257.3:c.4285_4287dup (MYH7) NP_000248.2:p.Met1429_Val1430insMet
NR_126491.1:n.852_854dup (MHRT)
XM_017021340.1:c.4285_4287dup (MYH7) XP_016876829.1:p.Met1429_Val1430insMet
NM_000257.4:c.4285_4287dup (MYH7) MANE Select NP_000248.2:p.Met1429_Val1430insMet