Canonical Allele Identifier: CA275937
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 208180
ClinVar RCV Id: RCV000190376
dbSNP Id: rs796064502

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894845G>T , CM000674.2:g.102894845G>T GRCh38
NC_000012.11:g.103288623G>T , CM000674.1:g.103288623G>T GRCh37
NC_000012.10:g.101812753G>T NCBI36
NG_008690.1:g.27758C>A
NG_008690.2:g.68566C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.242C>A MANE Select ENSP00000448059.1:p.Thr81Asn
ENST00000307000.7:c.227C>A ENSP00000303500.2:p.Thr76Asn
ENST00000546844.1:c.242C>A ENSP00000446658.1:p.Thr81Asn
ENST00000548677.2:n.329C>A
ENST00000548928.1:n.164C>A
ENST00000549111.5:n.338C>A
ENST00000550978.6:c.226C>A
ENST00000551337.5:c.242C>A ENSP00000447620.1:p.Thr81Asn
ENST00000551988.5:n.331C>A
ENST00000553106.5:c.242C>A ENSP00000448059.1:p.Thr81Asn
NM_000277.1:c.242C>A NP_000268.1:p.Thr81Asn
XM_011538422.1:c.242C>A XP_011536724.1:p.Thr81Asn
NM_000277.2:c.242C>A NP_000268.1:p.Thr81Asn
NM_001354304.1:c.242C>A NP_001341233.1:p.Thr81Asn
XM_017019370.2:c.242C>A XP_016874859.1:p.Thr81Asn
NM_000277.3:c.242C>A MANE Select NP_000268.1:p.Thr81Asn
NM_001354304.2:c.242C>A NP_001341233.1:p.Thr81Asn