Canonical Allele Identifier: CA242473148
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs140869484

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854269del , CM000674.2:g.102854269del GRCh38
NC_000012.11:g.103248047del , CM000674.1:g.103248047del GRCh37
NC_000012.10:g.101772177del NCBI36
NG_008690.1:g.68338del
NG_008690.2:g.109146del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.706+871del MANE Select ENSP00000448059.1:n.706+871del
ENST00000307000.7:c.691+871del ENSP00000303500.2:n.691+871del
ENST00000553106.5:c.706+871del ENSP00000448059.1:n.706+871del
NM_000277.1:c.706+871del NP_000268.1:n.706+871del
XM_011538422.1:c.706+871del XP_011536724.1:n.706+871del
NM_000277.2:c.706+871del NP_000268.1:n.706+871del
NM_001354304.1:c.706+871del NP_001341233.1:n.706+871del
XM_017019370.2:c.*520del XP_016874859.1:n.*520del
NM_000277.3:c.706+871del MANE Select NP_000268.1:n.706+871del
NM_001354304.2:c.706+871del NP_001341233.1:n.706+871del