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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:
CA91668546
Gene: MSX1
HGNC
NCBI
Linked Data
dbSNP Id:
rs997321662
gnomAD v4:
4-4860155-G-C
MyVariant Identifiers:
chr4:g.4861882G>C (hg19)
chr4:g.4860155G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.4860155G>C , CM000666.2:g.4860155G>C
GRCh38
NC_000004.11:g.4861882G>C , CM000666.1:g.4861882G>C
GRCh37
NC_000004.10:g.4912783G>C
NCBI36
NG_008121.1:g.5491G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000382723.5:c.256G>C
MANE Select
ENSP00000372170.4:p.Val86Leu
ENST00000382723.4:c.256G>C
ENSP00000372170.4:p.Val86Leu
NM_002448.3:c.256G>C
MANE Select
NP_002439.2:p.Val86Leu
Search 100 bp 5'
Search 100 bp 3'