Canonical Allele Identifier: CA386304024
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103288563T>G (hg19) chr12:g.102894785T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894785T>G , CM000674.2:g.102894785T>G GRCh38
NC_000012.11:g.103288563T>G , CM000674.1:g.103288563T>G GRCh37
NC_000012.10:g.101812693T>G NCBI36
NG_008690.1:g.27818A>C
NG_008690.2:g.68626A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.302A>C MANE Select ENSP00000448059.1:p.Asp101Ala
ENST00000307000.7:c.287A>C ENSP00000303500.2:p.Asp96Ala
ENST00000546844.1:c.302A>C ENSP00000446658.1:p.Asp101Ala
ENST00000548928.1:n.224A>C
ENST00000549111.5:n.398A>C
ENST00000550978.6:c.286A>C
ENST00000551337.5:c.302A>C ENSP00000447620.1:p.Asp101Ala
ENST00000551988.5:n.391A>C
ENST00000553106.5:c.302A>C ENSP00000448059.1:p.Asp101Ala
NM_000277.1:c.302A>C NP_000268.1:p.Asp101Ala
XM_011538422.1:c.302A>C XP_011536724.1:p.Asp101Ala
NM_000277.2:c.302A>C NP_000268.1:p.Asp101Ala
NM_001354304.1:c.302A>C NP_001341233.1:p.Asp101Ala
XM_017019370.2:c.302A>C XP_016874859.1:p.Asp101Ala
NM_000277.3:c.302A>C MANE Select NP_000268.1:p.Asp101Ala
NM_001354304.2:c.302A>C NP_001341233.1:p.Asp101Ala
Search 100 bp 5'
Search 100 bp 3'