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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:
CA403086095
Gene: MCOLN1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2708410
ClinVar RCV Id:
RCV003505924
MyVariant Identifiers:
chr19:g.7593795T>G (hg19)
chr19:g.7528909T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.7528909T>G , CM000681.2:g.7528909T>G
GRCh38
NC_000019.9:g.7593795T>G , CM000681.1:g.7593795T>G
GRCh37
NC_000019.8:g.7499795T>G
NCBI36
NG_015806.1:g.11300T>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000264079.11:c.1073T>G
MANE Select
ENSP00000264079.5:p.Leu358Arg
ENST00000264079.10:c.1073T>G
ENSP00000264079.5:p.Leu358Arg
ENST00000394321.9:n.1388T>G
ENST00000595860.5:n.256T>G
NM_020533.2:c.1073T>G
NP_065394.1:p.Leu358Arg
NM_020533.3:c.1073T>G
MANE Select
NP_065394.1:p.Leu358Arg
Search 100 bp 5'
Search 100 bp 3'