Canonical Allele Identifier: CA2538330466
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840252_102840253insCCTCCTACCA , CM000674.2:g.102840252_102840253insCCTCCTACCA GRCh38
NC_000012.11:g.103234030_103234031insCCTCCTACCA , CM000674.1:g.103234030_103234031insCCTCCTACCA GRCh37
NC_000012.10:g.101758160_101758161insCCTCCTACCA NCBI36
NG_008690.1:g.82353_82354insTAGGAGGTGG
NG_008690.2:g.123161_123162insTAGGAGGTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1315+150_1315+151insTAGGAGGTGG MANE Select ENSP00000448059.1:n.1315+150_1315+151insT...
ENST00000307000.7:c.1300+150_1300+151insTAGGAGGTGG ENSP00000303500.2:n.1300+150_1300+151insT...
ENST00000551114.2:n.977+150_977+151insTAGGAGGTGG
ENST00000553106.5:c.1315+150_1315+151insTAGGAGGTGG ENSP00000448059.1:n.1315+150_1315+151insT...
ENST00000635477.1:c.419+150_419+151insTAGGAGGTGG
ENST00000635528.1:n.830+150_830+151insTAGGAGGTGG
NM_000277.1:c.1315+150_1315+151insTAGGAGGTGG NP_000268.1:n.1315+150_1315+151insTAGGAGG...
XM_011538422.1:c.1258+150_1258+151insTAGGAGGTGG XP_011536724.1:n.1258+150_1258+151insTAGG...
NM_000277.2:c.1315+150_1315+151insTAGGAGGTGG NP_000268.1:n.1315+150_1315+151insTAGGAGG...
NM_001354304.1:c.1315+150_1315+151insTAGGAGGTGG NP_001341233.1:n.1315+150_1315+151insTAGG...
NM_000277.3:c.1315+150_1315+151insTAGGAGGTGG MANE Select NP_000268.1:n.1315+150_1315+151insTAGGAGG...
NM_001354304.2:c.1315+150_1315+151insTAGGAGGTGG NP_001341233.1:n.1315+150_1315+151insTAGG...