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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:
CA367069326
Gene: HOXA1
HGNC
NCBI
Linked Data
dbSNP Id:
rs751378994
MyVariant Identifiers:
chr7:g.27135348C>A (hg19)
chr7:g.27095729C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.27095729C>A , CM000669.2:g.27095729C>A
GRCh38
NC_000007.13:g.27135348C>A , CM000669.1:g.27135348C>A
GRCh37
NC_000007.12:g.27101873C>A
NCBI36
NG_011813.1:g.5278G>T
NG_033087.1:g.4636C>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000643460.2:c.184G>T
MANE Select
ENSP00000494260.2:p.Gly62Cys
ENST00000343060.4:c.184G>T
ENSP00000343246.4:p.Gly62Cys
ENST00000355633.5:c.184G>T
ENSP00000347851.5:p.Gly62Cys
NM_005522.4:c.184G>T
NP_005513.1:p.Gly62Cys
NM_153620.2:c.184G>T
NP_705873.2:p.Gly62Cys
NM_005522.5:c.184G>T
MANE Select
NP_005513.2:p.Gly62Cys
NM_153620.3:c.184G>T
NP_705873.3:p.Gly62Cys
Search 100 bp 5'
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