Canonical Allele Identifier: CA951246721
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1876613831

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877419dup , CM000674.2:g.102877419dup GRCh38
NC_000012.11:g.103271197dup , CM000674.1:g.103271197dup GRCh37
NC_000012.10:g.101795327dup NCBI36
NG_008690.1:g.45185dup
NG_008690.2:g.85993dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.441+44dup MANE Select ENSP00000448059.1:n.441+44dup
ENST00000307000.7:c.426+44dup ENSP00000303500.2:n.426+44dup
ENST00000549111.5:n.537+44dup
ENST00000550978.6:c.469dup
ENST00000551988.5:n.530+44dup
ENST00000553106.5:c.441+44dup ENSP00000448059.1:n.441+44dup
NM_000277.1:c.441+44dup NP_000268.1:n.441+44dup
XM_011538422.1:c.441+44dup XP_011536724.1:n.441+44dup
NM_000277.2:c.441+44dup NP_000268.1:n.441+44dup
NM_001354304.1:c.441+44dup NP_001341233.1:n.441+44dup
XM_017019370.2:c.441+44dup XP_016874859.1:n.441+44dup
NM_000277.3:c.441+44dup MANE Select NP_000268.1:n.441+44dup
NM_001354304.2:c.441+44dup NP_001341233.1:n.441+44dup