Canonical Allele Identifier: CA386304256
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103288688A>C (hg19) chr12:g.102894910A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894910A>C , CM000674.2:g.102894910A>C GRCh38
NC_000012.11:g.103288688A>C , CM000674.1:g.103288688A>C GRCh37
NC_000012.10:g.101812818A>C NCBI36
NG_008690.1:g.27693T>G
NG_008690.2:g.68501T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.177T>G MANE Select ENSP00000448059.1:p.Asp59Glu
ENST00000307000.7:c.162T>G ENSP00000303500.2:p.Asp54Glu
ENST00000546844.1:c.177T>G ENSP00000446658.1:p.Asp59Glu
ENST00000548677.2:n.264T>G
ENST00000548928.1:n.99T>G
ENST00000549111.5:n.273T>G
ENST00000550978.6:c.161T>G
ENST00000551337.5:c.177T>G ENSP00000447620.1:p.Asp59Glu
ENST00000551988.5:n.266T>G
ENST00000553106.5:c.177T>G ENSP00000448059.1:p.Asp59Glu
ENST00000635500.1:n.145T>G
NM_000277.1:c.177T>G NP_000268.1:p.Asp59Glu
XM_011538422.1:c.177T>G XP_011536724.1:p.Asp59Glu
NM_000277.2:c.177T>G NP_000268.1:p.Asp59Glu
NM_001354304.1:c.177T>G NP_001341233.1:p.Asp59Glu
XM_017019370.2:c.177T>G XP_016874859.1:p.Asp59Glu
NM_000277.3:c.177T>G MANE Select NP_000268.1:p.Asp59Glu
NM_001354304.2:c.177T>G NP_001341233.1:p.Asp59Glu
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