Canonical Allele Identifier: CA2624234738
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422412_23422435dup , CM000676.2:g.23422412_23422435dup GRCh38
NC_000014.8:g.23891621_23891644dup , CM000676.1:g.23891621_23891644dup GRCh37
NC_000014.7:g.22961461_22961484dup NCBI36
NG_007884.1:g.18230_18253dup , LRG_384:g.18230_18253dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-107_3100-84dup MANE Select ENSP00000347507.3:n.3100-107_3100-84dup
ENST00000355349.3:c.3100-107_3100-84dup ENSP00000347507.3:n.3100-107_3100-84dup
NM_000257.3:c.3100-107_3100-84dup NP_000248.2:n.3100-107_3100-84dup
XR_245686.3:n.3206-107_3206-84dup
XM_017021340.1:c.3100-107_3100-84dup XP_016876829.1:n.3100-107_3100-84dup
NM_000257.4:c.3100-107_3100-84dup MANE Select NP_000248.2:n.3100-107_3100-84dup