Canonical Allele Identifier: CA2620506391
Community Standard Title: NM_000277.3(PAH):c.1199+151T>G
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843495A>C , CM000674.2:g.102843495A>C GRCh38
NC_000012.11:g.103237273A>C , CM000674.1:g.103237273A>C GRCh37
NC_000012.10:g.101761403A>C NCBI36
NG_008690.1:g.79108T>G
NG_008690.2:g.119916T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.1199+151T>G MANE Select NP_000268.1:n.1199+151T>G
ENST00000553106.6:c.1199+151T>G MANE Select ENSP00000448059.1:n.1199+151T>G
NM_000277.1:c.1199+151T>G NP_000268.1:n.1199+151T>G
NM_000277.2:c.1199+151T>G NP_000268.1:n.1199+151T>G
NM_001354304.1:c.1199+151T>G NP_001341233.1:n.1199+151T>G
NM_001354304.2:c.1199+151T>G NP_001341233.1:n.1199+151T>G
ENST00000307000.7:c.1184+151T>G ENSP00000303500.2:n.1184+151T>G
ENST00000549247.6:n.958+151T>G
ENST00000551114.2:n.861+151T>G
ENST00000553106.5:c.1199+151T>G ENSP00000448059.1:n.1199+151T>G
ENST00000635477.1:c.303+151T>G
ENST00000635528.1:n.714+151T>G
XM_011538422.1:c.1142+151T>G XP_011536724.1:n.1142+151T>G
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