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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:
CA386013764
Gene: KERA
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr12:g.91449464T>C (hg19)
chr12:g.91055687T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.91055687T>C , CM000674.2:g.91055687T>C
GRCh38
NC_000012.11:g.91449464T>C , CM000674.1:g.91449464T>C
GRCh37
NC_000012.10:g.89973595T>C
NCBI36
NG_021223.1:g.7668A>G , LRG_538:g.7668A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000266719.4:c.595A>G
MANE Select
ENSP00000266719.3:p.Met199Val
ENST00000266719.3:c.595A>G
ENSP00000266719.3:p.Met199Val
NM_007035.3:c.595A>G , LRG_538t1:c.595A>G
NP_008966.1:p.Met199Val
XM_011537781.1:c.595A>G
XP_011536083.1:p.Met199Val
NM_007035.4:c.595A>G
MANE Select
NP_008966.1:p.Met199Val
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