Canonical Allele Identifier: CA041696

Linked Data

ClinVar Variation Id: 263348
dbSNP Id: rs182311329

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417509G>A , CM000676.2:g.23417509G>A GRCh38
NC_000014.8:g.23886718G>A , CM000676.1:g.23886718G>A GRCh37
NC_000014.7:g.22956558G>A NCBI36
NG_007884.1:g.23153C>T , LRG_384:g.23153C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4347C>T (MYH7) MANE Select ENSP00000347507.3:p.Phe1449=
ENST00000355349.3:c.4347C>T (MYH7) ENSP00000347507.3:p.Phe1449=
NM_000257.3:c.4347C>T (MYH7) NP_000248.2:p.Phe1449=
NR_126491.1:n.814-24G>A (MHRT)
XM_017021340.1:c.4347C>T (MYH7) XP_016876829.1:p.Phe1449=
NM_000257.4:c.4347C>T (MYH7) MANE Select NP_000248.2:p.Phe1449=