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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:
CA403091531
Gene: MCOLN1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr19:g.7598463T>C (hg19)
chr19:g.7533577T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.7533577T>C , CM000681.2:g.7533577T>C
GRCh38
NC_000019.9:g.7598463T>C , CM000681.1:g.7598463T>C
GRCh37
NC_000019.8:g.7504463T>C
NCBI36
NG_013374.1:g.4426T>C
NG_015806.1:g.15968T>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000264079.11:c.1630T>C
MANE Select
ENSP00000264079.5:p.Cys544Arg
ENST00000264079.10:c.1630T>C
ENSP00000264079.5:p.Cys544Arg
ENST00000394321.9:n.1945T>C
ENST00000599334.1:c.358T>C
ENST00000602227.1:n.184T>C
NM_020533.2:c.1630T>C
NP_065394.1:p.Cys544Arg
NM_020533.3:c.1630T>C
MANE Select
NP_065394.1:p.Cys544Arg
Search 100 bp 5'
Search 100 bp 3'