Canonical Allele Identifier: CA015240

Linked Data

ClinVar Variation Id: 191727
ClinVar RCV Id: RCV000172043
dbSNP Id: rs199557822

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416250C>A , CM000676.2:g.23416250C>A GRCh38
NC_000014.8:g.23885459C>A , CM000676.1:g.23885459C>A GRCh37
NC_000014.7:g.22955299C>A NCBI36
NG_007884.1:g.24412G>T , LRG_384:g.24412G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4707G>T (MYH7) MANE Select ENSP00000347507.3:p.Lys1569Asn
ENST00000355349.3:c.4707G>T (MYH7) ENSP00000347507.3:p.Lys1569Asn
NM_000257.3:c.4707G>T (MYH7) NP_000248.2:p.Lys1569Asn
NR_126491.1:n.511C>A (MHRT)
XM_017021340.1:c.4707G>T (MYH7) XP_016876829.1:p.Lys1569Asn
NM_000257.4:c.4707G>T (MYH7) MANE Select NP_000248.2:p.Lys1569Asn