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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:
CA247528421
Gene: KL
HGNC
NCBI
Linked Data
dbSNP Id:
rs9536314
MyVariant Identifiers:
chr13:g.33628138T>A (hg19)
chr13:g.33054001T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.33054001T>A , CM000675.2:g.33054001T>A
GRCh38
NC_000013.10:g.33628138T>A , CM000675.1:g.33628138T>A
GRCh37
NC_000013.9:g.32526138T>A
NCBI36
NG_011485.1:g.42568T>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000380099.4:c.1054T>A
MANE Select
ENSP00000369442.3:p.Phe352Ile
ENST00000380099.3:c.1054T>A
ENSP00000369442.3:p.Phe352Ile
ENST00000487852.1:n.1062T>A
NM_004795.3:c.1054T>A
NP_004786.2:p.Phe352Ile
XM_006719895.1:c.133T>A
XP_006719958.1:p.Phe45Ile
XM_006719895.2:c.133T>A
XP_006719958.1:p.Phe45Ile
NM_004795.4:c.1054T>A
MANE Select
NP_004786.2:p.Phe352Ile
Search 100 bp 5'
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