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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:
CA121679131
Gene: ARSB
HGNC
NCBI
Linked Data
dbSNP Id:
rs267600697
MyVariant Identifiers:
chr5:g.78076279G>A (hg19)
chr5:g.78780456G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.78780456G>A , CM000667.2:g.78780456G>A
GRCh38
NC_000005.9:g.78076279G>A , CM000667.1:g.78076279G>A
GRCh37
NC_000005.8:g.78112035G>A
NCBI36
NG_007089.1:g.211079C>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000264914.10:c.1543C>T
MANE Select
ENSP00000264914.4:p.Pro515Ser
ENST00000264914.8:c.1543C>T
ENSP00000264914.4:p.Pro515Ser
ENST00000521011.1:n.508C>T
NM_000046.3:c.1543C>T
NP_000037.2:p.Pro515Ser
XM_011543390.1:c.1543C>T
XP_011541692.1:p.Pro515Ser
NM_000046.4:c.1543C>T
NP_000037.2:p.Pro515Ser
NM_000046.5:c.1543C>T
MANE Select
NP_000037.2:p.Pro515Ser
Search 100 bp 5'
Search 100 bp 3'