Canonical Allele Identifier: CA2620507639
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102894697-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894697T>G , CM000674.2:g.102894697T>G GRCh38
NC_000012.11:g.103288475T>G , CM000674.1:g.103288475T>G GRCh37
NC_000012.10:g.101812605T>G NCBI36
NG_008690.1:g.27906A>C
NG_008690.2:g.68714A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.352+38A>C MANE Select ENSP00000448059.1:n.352+38A>C
ENST00000307000.7:c.337+38A>C ENSP00000303500.2:n.337+38A>C
ENST00000548928.1:n.274+38A>C
ENST00000549111.5:n.448+38A>C
ENST00000550978.6:c.336+38A>C
ENST00000551337.5:c.352+38A>C ENSP00000447620.1:n.352+38A>C
ENST00000551988.5:n.441+38A>C
ENST00000553106.5:c.352+38A>C ENSP00000448059.1:n.352+38A>C
NM_000277.1:c.352+38A>C NP_000268.1:n.352+38A>C
XM_011538422.1:c.352+38A>C XP_011536724.1:n.352+38A>C
NM_000277.2:c.352+38A>C NP_000268.1:n.352+38A>C
NM_001354304.1:c.352+38A>C NP_001341233.1:n.352+38A>C
XM_017019370.2:c.352+38A>C XP_016874859.1:n.352+38A>C
NM_000277.3:c.352+38A>C MANE Select NP_000268.1:n.352+38A>C
NM_001354304.2:c.352+38A>C NP_001341233.1:n.352+38A>C
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