Canonical Allele Identifier: CA389037831

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416258G>T , CM000676.2:g.23416258G>T GRCh38
NC_000014.8:g.23885467G>T , CM000676.1:g.23885467G>T GRCh37
NC_000014.7:g.22955307G>T NCBI36
NG_007884.1:g.24404C>A , LRG_384:g.24404C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4699C>A (MYH7) MANE Select ENSP00000347507.3:p.Gln1567Lys
ENST00000355349.3:c.4699C>A (MYH7) ENSP00000347507.3:p.Gln1567Lys
NM_000257.3:c.4699C>A (MYH7) NP_000248.2:p.Gln1567Lys
NR_126491.1:n.519G>T (MHRT)
XM_017021340.1:c.4699C>A (MYH7) XP_016876829.1:p.Gln1567Lys
NM_000257.4:c.4699C>A (MYH7) MANE Select NP_000248.2:p.Gln1567Lys