Canonical Allele Identifier: CA389039982
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2105624
ClinVar RCV Id: RCV003023550
MyVariant Identifiers: chr14:g.23886713T>G (hg19) chr14:g.23417504T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417504T>G , CM000676.2:g.23417504T>G GRCh38
NC_000014.8:g.23886713T>G , CM000676.1:g.23886713T>G GRCh37
NC_000014.7:g.22956553T>G NCBI36
NG_007884.1:g.23158A>C , LRG_384:g.23158A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4352A>C (MYH7) MANE Select ENSP00000347507.3:p.Lys1451Thr
ENST00000355349.3:c.4352A>C (MYH7) ENSP00000347507.3:p.Lys1451Thr
NM_000257.3:c.4352A>C (MYH7) NP_000248.2:p.Lys1451Thr
NR_126491.1:n.814-29T>G (MHRT)
XM_017021340.1:c.4352A>C (MYH7) XP_016876829.1:p.Lys1451Thr
NM_000257.4:c.4352A>C (MYH7) MANE Select NP_000248.2:p.Lys1451Thr
Search 100 bp 5'
Search 100 bp 3'