Canonical Allele Identifier: CA2620525715
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102854853-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854855del , CM000674.2:g.102854855del GRCh38
NC_000012.11:g.103248633del , CM000674.1:g.103248633del GRCh37
NC_000012.10:g.101772763del NCBI36
NG_008690.1:g.67749del
NG_008690.2:g.108557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.706+282del MANE Select ENSP00000448059.1:n.706+282del
ENST00000307000.7:c.691+282del ENSP00000303500.2:n.691+282del
ENST00000549111.5:n.1084del
ENST00000553106.5:c.706+282del ENSP00000448059.1:n.706+282del
NM_000277.1:c.706+282del NP_000268.1:n.706+282del
XM_011538422.1:c.706+282del XP_011536724.1:n.706+282del
NM_000277.2:c.706+282del NP_000268.1:n.706+282del
NM_001354304.1:c.706+282del NP_001341233.1:n.706+282del
XM_017019370.2:c.707-53del XP_016874859.1:n.707-53del
NM_000277.3:c.706+282del MANE Select NP_000268.1:n.706+282del
NM_001354304.2:c.706+282del NP_001341233.1:n.706+282del
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