Canonical Allele Identifier: CA2059449698
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855290_102855291delinsCT , CM000674.2:g.102855290_102855291delinsCT GRCh38
NC_000012.11:g.103249068_103249069delinsCT , CM000674.1:g.103249068_103249069delinsCT GRCh37
NC_000012.10:g.101773198_101773199delinsCT NCBI36
NG_008690.1:g.67312_67313delinsAG
NG_008690.2:g.108120_108121delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.551_552delinsAG MANE Select ENSP00000448059.1:p.Lys184=
ENST00000307000.7:c.536_537delinsAG ENSP00000303500.2:p.Lys179=
ENST00000549111.5:n.647_648delinsAG
ENST00000551988.5:n.572_573delinsAG
ENST00000553106.5:c.551_552delinsAG ENSP00000448059.1:p.Lys184=
NM_000277.1:c.551_552delinsAG NP_000268.1:p.Lys184=
XM_011538422.1:c.551_552delinsAG XP_011536724.1:p.Lys184=
NM_000277.2:c.551_552delinsAG NP_000268.1:p.Lys184=
NM_001354304.1:c.551_552delinsAG NP_001341233.1:p.Lys184=
XM_017019370.2:c.551_552delinsAG XP_016874859.1:p.Lys184=
NM_000277.3:c.551_552delinsAG MANE Select NP_000268.1:p.Lys184=
NM_001354304.2:c.551_552delinsAG NP_001341233.1:p.Lys184=