Canonical Allele Identifier: CA386302670
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103306651C>T (hg19) chr12:g.102912873C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102912873C>T , CM000674.2:g.102912873C>T GRCh38
NC_000012.11:g.103306651C>T , CM000674.1:g.103306651C>T GRCh37
NC_000012.10:g.101830781C>T NCBI36
NG_008690.1:g.9730G>A
NG_008690.2:g.50538G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.86G>A MANE Select ENSP00000448059.1:p.Cys29Tyr
ENST00000307000.7:c.71G>A ENSP00000303500.2:p.Cys24Tyr
ENST00000546844.1:c.86G>A ENSP00000446658.1:p.Cys29Tyr
ENST00000548677.2:n.173G>A
ENST00000548928.1:n.8G>A
ENST00000549111.5:n.182G>A
ENST00000550978.6:c.70G>A
ENST00000551337.5:c.86G>A ENSP00000447620.1:p.Cys29Tyr
ENST00000551988.5:n.175G>A
ENST00000553106.5:c.86G>A ENSP00000448059.1:p.Cys29Tyr
ENST00000635500.1:n.54G>A
NM_000277.1:c.86G>A NP_000268.1:p.Cys29Tyr
XM_011538422.1:c.86G>A XP_011536724.1:p.Cys29Tyr
NM_000277.2:c.86G>A NP_000268.1:p.Cys29Tyr
NM_001354304.1:c.86G>A NP_001341233.1:p.Cys29Tyr
XM_017019370.2:c.86G>A XP_016874859.1:p.Cys29Tyr
NM_000277.3:c.86G>A MANE Select NP_000268.1:p.Cys29Tyr
NM_001354304.2:c.86G>A NP_001341233.1:p.Cys29Tyr
Search 100 bp 5'
Search 100 bp 3'