Canonical Allele Identifier: CA2059448204
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854456_102854461delinsTGTACA , CM000674.2:g.102854456_102854461delinsTGTACA GRCh38
NC_000012.11:g.103248234_103248239delinsTGTACA , CM000674.1:g.103248234_103248239delinsTGTACA GRCh37
NC_000012.10:g.101772364_101772369delinsTGTACA NCBI36
NG_008690.1:g.68142_68147delinsTGTACA
NG_008690.2:g.108950_108955delinsTGTACA

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.706+675_706+680delinsTGTACA MANE Select ENSP00000448059.1:n.706+675_706+680delins...
ENST00000307000.7:c.691+675_691+680delinsTGTACA ENSP00000303500.2:n.691+675_691+680delins...
ENST00000553106.5:c.706+675_706+680delinsTGTACA ENSP00000448059.1:n.706+675_706+680delins...
NM_000277.1:c.706+675_706+680delinsTGTACA NP_000268.1:n.706+675_706+680delinsTGTACA...
XM_011538422.1:c.706+675_706+680delinsTGTACA XP_011536724.1:n.706+675_706+680delinsTGT...
NM_000277.2:c.706+675_706+680delinsTGTACA NP_000268.1:n.706+675_706+680delinsTGTACA...
NM_001354304.1:c.706+675_706+680delinsTGTACA NP_001341233.1:n.706+675_706+680delinsTGT...
XM_017019370.2:c.*324_*329delinsTGTACA XP_016874859.1:n.*324_*329delinsTGTACA
NM_000277.3:c.706+675_706+680delinsTGTACA MANE Select NP_000268.1:n.706+675_706+680delinsTGTACA...
NM_001354304.2:c.706+675_706+680delinsTGTACA NP_001341233.1:n.706+675_706+680delinsTGT...