Canonical Allele Identifier: CA386291562
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846906T>G , CM000674.2:g.102846906T>G GRCh38
NC_000012.11:g.103240684T>G , CM000674.1:g.103240684T>G GRCh37
NC_000012.10:g.101764814T>G NCBI36
NG_008690.1:g.75697A>C
NG_008690.2:g.116505A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.958A>C MANE Select ENSP00000448059.1:p.Lys320Gln
ENST00000307000.7:c.943A>C ENSP00000303500.2:p.Lys315Gln
ENST00000549247.6:n.717A>C
ENST00000551114.2:n.620A>C
ENST00000553106.5:c.958A>C ENSP00000448059.1:p.Lys320Gln
ENST00000635477.1:n.74-2475A>C
ENST00000635528.1:n.473A>C
NM_000277.1:c.958A>C NP_000268.1:p.Lys320Gln
XM_011538422.1:c.913-2475A>C XP_011536724.1:n.913-2475A>C
NM_000277.2:c.958A>C NP_000268.1:p.Lys320Gln
NM_001354304.1:c.958A>C NP_001341233.1:p.Lys320Gln
NM_000277.3:c.958A>C MANE Select NP_000268.1:p.Lys320Gln
NM_001354304.2:c.958A>C NP_001341233.1:p.Lys320Gln