Canonical Allele Identifier: CA2624236938

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417151_23417162dup , CM000676.2:g.23417151_23417162dup GRCh38
NC_000014.8:g.23886360_23886371dup , CM000676.1:g.23886360_23886371dup GRCh37
NC_000014.7:g.22956200_22956211dup NCBI36
NG_007884.1:g.23500_23511dup , LRG_384:g.23500_23511dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4510_4519+2dup (MYH7)
ENST00000355349.3:c.4510_4519+2dup (MYH7)
NM_000257.3:c.4510_4519+2dup (MYH7)
NR_126491.1:n.652-61_652-50dup (MHRT)
XM_017021340.1:c.4510_4519+2dup (MYH7)
NM_000257.4:c.4510_4519+2dup (MYH7)