Canonical Allele Identifier: CA485617770

Linked Data

ClinVar Variation Id: 743258
ClinVar RCV Id: RCV001426099
dbSNP Id: rs1595075231
MyVariant Identifiers: chr14:g.23886751A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417542A>G , CM000676.2:g.23417542A>G GRCh38
NC_000014.8:g.23886751A>G , CM000676.1:g.23886751A>G GRCh37
NC_000014.7:g.22956591A>G NCBI36
NG_007884.1:g.23120T>C , LRG_384:g.23120T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4314T>C (MYH7) MANE Select ENSP00000347507.3:p.Ala1438=
ENST00000355349.3:c.4314T>C (MYH7) ENSP00000347507.3:p.Ala1438=
NM_000257.3:c.4314T>C (MYH7) NP_000248.2:p.Ala1438=
NR_126491.1:n.823A>G (MHRT)
XM_017021340.1:c.4314T>C (MYH7) XP_016876829.1:p.Ala1438=
NM_000257.4:c.4314T>C (MYH7) MANE Select NP_000248.2:p.Ala1438=