Canonical Allele Identifier: CA2620507350
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102877448-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877448G>T , CM000674.2:g.102877448G>T GRCh38
NC_000012.11:g.103271226G>T , CM000674.1:g.103271226G>T GRCh37
NC_000012.10:g.101795356G>T NCBI36
NG_008690.1:g.45155C>A
NG_008690.2:g.85963C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.441+14C>A MANE Select ENSP00000448059.1:n.441+14C>A
ENST00000307000.7:c.426+14C>A ENSP00000303500.2:n.426+14C>A
ENST00000549111.5:n.537+14C>A
ENST00000550978.6:c.439C>A
ENST00000551988.5:n.530+14C>A
ENST00000553106.5:c.441+14C>A ENSP00000448059.1:n.441+14C>A
NM_000277.1:c.441+14C>A NP_000268.1:n.441+14C>A
XM_011538422.1:c.441+14C>A XP_011536724.1:n.441+14C>A
NM_000277.2:c.441+14C>A NP_000268.1:n.441+14C>A
NM_001354304.1:c.441+14C>A NP_001341233.1:n.441+14C>A
XM_017019370.2:c.441+14C>A XP_016874859.1:n.441+14C>A
NM_000277.3:c.441+14C>A MANE Select NP_000268.1:n.441+14C>A
NM_001354304.2:c.441+14C>A NP_001341233.1:n.441+14C>A
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