Canonical Allele Identifier: CA10581171
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 235032
ClinVar RCV Id: RCV000223810 RCV001187347 RCV001577895 RCV001854769 RCV002327098
dbSNP Id: rs876661373
gnomAD v2: 14-23886518-C-T
gnomAD v3: 14-23417309-C-T
gnomAD v4: 14-23417309-C-T
COSMIC: COSM2031775
MyVariant Identifiers: chr14:g.23886518C>T (hg19) chr14:g.23417309C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417309C>T , CM000676.2:g.23417309C>T GRCh38
NC_000014.8:g.23886518C>T , CM000676.1:g.23886518C>T GRCh37
NC_000014.7:g.22956358C>T NCBI36
NG_007884.1:g.23353G>A , LRG_384:g.23353G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4363G>A (MYH7) MANE Select ENSP00000347507.3:p.Glu1455Lys
ENST00000355349.3:c.4363G>A (MYH7) ENSP00000347507.3:p.Glu1455Lys
NM_000257.3:c.4363G>A (MYH7) NP_000248.2:p.Glu1455Lys
NR_126491.1:n.749C>T (MHRT)
XM_017021340.1:c.4363G>A (MYH7) XP_016876829.1:p.Glu1455Lys
NM_000257.4:c.4363G>A (MYH7) MANE Select NP_000248.2:p.Glu1455Lys
Search 100 bp 5'
Search 100 bp 3'