Canonical Allele Identifier: CA312809
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 203874
ClinVar RCV Id: RCV000186078
dbSNP Id: rs796052017

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852922_102852923delinsTG , CM000674.2:g.102852922_102852923delinsTG GRCh38
NC_000012.11:g.103246700_103246701delinsTG , CM000674.1:g.103246700_103246701delinsTG GRCh37
NC_000012.10:g.101770830_101770831delinsTG NCBI36
NG_008690.1:g.69680_69681delinsCA
NG_008690.2:g.110488_110489delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.734_735delinsCA MANE Select ENSP00000448059.1:p.Val245Ala
ENST00000307000.7:c.719_720delinsCA ENSP00000303500.2:p.Val240Ala
ENST00000549247.6:n.493_494delinsCA
ENST00000553106.5:c.734_735delinsCA ENSP00000448059.1:p.Val245Ala
NM_000277.1:c.734_735delinsCA NP_000268.1:p.Val245Ala
XM_011538422.1:c.734_735delinsCA XP_011536724.1:p.Val245Ala
NM_000277.2:c.734_735delinsCA NP_000268.1:p.Val245Ala
NM_001354304.1:c.734_735delinsCA NP_001341233.1:p.Val245Ala
NM_000277.3:c.734_735delinsCA MANE Select NP_000268.1:p.Val245Ala
NM_001354304.2:c.734_735delinsCA NP_001341233.1:p.Val245Ala