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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA012894
Gene: MYH7
HGNC
NCBI
Linked Data
ClinVar Variation Id:
181202
ClinVar RCV Id:
RCV000768487
RCV003313941
RCV003332128
dbSNP Id:
rs730880756
MyVariant Identifiers:
chr14:g.23893331C>T (hg19)
chr14:g.23424122C>T (hg38)
ERepo:
CA012894/MONDO:0005045/002
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23424122C>T , CM000676.2:g.23424122C>T
GRCh38
NC_000014.8:g.23893331C>T , CM000676.1:g.23893331C>T
GRCh37
NC_000014.7:g.22963171C>T
NCBI36
NG_007884.1:g.16540G>A , LRG_384:g.16540G>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000355349.4:c.2707G>A
MANE Select
ENSP00000347507.3:p.Glu903Lys
ENST00000355349.3:c.2707G>A
ENSP00000347507.3:p.Glu903Lys
NM_000257.3:c.2707G>A
NP_000248.2:p.Glu903Lys
XR_245686.3:n.2813G>A
XM_017021340.1:c.2707G>A
XP_016876829.1:p.Glu903Lys
NM_000257.4:c.2707G>A
MANE Select
NP_000248.2:p.Glu903Lys
Search 100 bp 5'
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