Canonical Allele Identifier: CA386291660
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103240702G>C (hg19) chr12:g.102846924G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846924G>C , CM000674.2:g.102846924G>C GRCh38
NC_000012.11:g.103240702G>C , CM000674.1:g.103240702G>C GRCh37
NC_000012.10:g.101764832G>C NCBI36
NG_008690.1:g.75679C>G
NG_008690.2:g.116487C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.940C>G MANE Select ENSP00000448059.1:p.Pro314Ala
ENST00000307000.7:c.925C>G ENSP00000303500.2:p.Pro309Ala
ENST00000549247.6:n.699C>G
ENST00000551114.2:n.602C>G
ENST00000553106.5:c.940C>G ENSP00000448059.1:p.Pro314Ala
ENST00000635477.1:c.74-2493C>G
ENST00000635528.1:n.455C>G
NM_000277.1:c.940C>G NP_000268.1:p.Pro314Ala
XM_011538422.1:c.913-2493C>G XP_011536724.1:n.913-2493C>G
NM_000277.2:c.940C>G NP_000268.1:p.Pro314Ala
NM_001354304.1:c.940C>G NP_001341233.1:p.Pro314Ala
NM_000277.3:c.940C>G MANE Select NP_000268.1:p.Pro314Ala
NM_001354304.2:c.940C>G NP_001341233.1:p.Pro314Ala
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