Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

ClinGen Allele Registry

Canonical Allele Identifier: CA229684

Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102778

ClinVar RCV Id: RCV000089029

dbSNP Id: rs199475576

MyVariant Identifiers: chr12:g.103248948A>C (hg19) chr12:g.102855170A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102855170A>C , CM000674.2:g.102855170A>C	GRCh38
NC_000012.11:g.103248948A>C , CM000674.1:g.103248948A>C	GRCh37
NC_000012.10:g.101773078A>C	NCBI36
NG_008690.1:g.67433T>G
NG_008690.2:g.108241T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.672T>G MANE Select	ENSP00000448059.1:p.Ile224Met
ENST00000307000.7:c.657T>G	ENSP00000303500.2:p.Ile219Met
ENST00000549111.5:n.768T>G
ENST00000553106.5:c.672T>G	ENSP00000448059.1:p.Ile224Met
NM_000277.1:c.672T>G	NP_000268.1:p.Ile224Met
XM_011538422.1:c.672T>G	XP_011536724.1:p.Ile224Met
NM_000277.2:c.672T>G	NP_000268.1:p.Ile224Met
NM_001354304.1:c.672T>G	NP_001341233.1:p.Ile224Met
XM_017019370.2:c.672T>G	XP_016874859.1:p.Ile224Met
NM_000277.3:c.672T>G MANE Select	NP_000268.1:p.Ile224Met
NM_001354304.2:c.672T>G	NP_001341233.1:p.Ile224Met