Canonical Allele Identifier: CA389037334

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416030C>A , CM000676.2:g.23416030C>A GRCh38
NC_000014.8:g.23885239C>A , CM000676.1:g.23885239C>A GRCh37
NC_000014.7:g.22955079C>A NCBI36
NG_007884.1:g.24632G>T , LRG_384:g.24632G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4927G>T (MYH7) MANE Select ENSP00000347507.3:p.Val1643Phe
ENST00000355349.3:c.4927G>T (MYH7) ENSP00000347507.3:p.Val1643Phe
NM_000257.3:c.4927G>T (MYH7) NP_000248.2:p.Val1643Phe
NR_126491.1:n.291C>A (MHRT)
XM_017021340.1:c.4927G>T (MYH7) XP_016876829.1:p.Val1643Phe
NM_000257.4:c.4927G>T (MYH7) MANE Select NP_000248.2:p.Val1643Phe