Canonical Allele Identifier: CA961069623

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417417_23417419dup , CM000676.2:g.23417417_23417419dup GRCh38
NC_000014.8:g.23886626_23886628dup , CM000676.1:g.23886626_23886628dup GRCh37
NC_000014.7:g.22956466_22956468dup NCBI36
NG_007884.1:g.23245_23247dup , LRG_384:g.23245_23247dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+86_4353+88dup (MYH7) MANE Select ENSP00000347507.3:n.4353+86_4353+88dup
ENST00000355349.3:c.4353+86_4353+88dup (MYH7) ENSP00000347507.3:n.4353+86_4353+88dup
NM_000257.3:c.4353+86_4353+88dup (MYH7) NP_000248.2:n.4353+86_4353+88dup
NR_126491.1:n.813+44_813+46dup (MHRT)
XM_017021340.1:c.4353+86_4353+88dup (MYH7) XP_016876829.1:n.4353+86_4353+88dup
NM_000257.4:c.4353+86_4353+88dup (MYH7) MANE Select NP_000248.2:n.4353+86_4353+88dup