Canonical Allele Identifier: CA2575266782
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844485T>C , CM000674.2:g.102844485T>C GRCh38
NC_000012.11:g.103238263T>C , CM000674.1:g.103238263T>C GRCh37
NC_000012.10:g.101762393T>C NCBI36
NG_008690.1:g.78118A>G
NG_008690.2:g.118926A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.970-54A>G MANE Select ENSP00000448059.1:n.970-54A>G
ENST00000307000.7:c.955-54A>G ENSP00000303500.2:n.955-54A>G
ENST00000549247.6:n.729-54A>G
ENST00000551114.2:n.632-54A>G
ENST00000553106.5:c.970-54A>G ENSP00000448059.1:n.970-54A>G
ENST00000635477.1:c.74-54A>G
ENST00000635528.1:n.485-54A>G
NM_000277.1:c.970-54A>G NP_000268.1:n.970-54A>G
XM_011538422.1:c.913-54A>G XP_011536724.1:n.913-54A>G
NM_000277.2:c.970-54A>G NP_000268.1:n.970-54A>G
NM_001354304.1:c.970-54A>G NP_001341233.1:n.970-54A>G
NM_000277.3:c.970-54A>G MANE Select NP_000268.1:n.970-54A>G
NM_001354304.2:c.970-54A>G NP_001341233.1:n.970-54A>G
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