Canonical Allele Identifier: CA2059451083
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846764_102846769delinsAAATGT , CM000674.2:g.102846764_102846769delinsAAATGT GRCh38
NC_000012.11:g.103240542_103240547delinsAAATGT , CM000674.1:g.103240542_103240547delinsAAATGT GRCh37
NC_000012.10:g.101764672_101764677delinsAAATGT NCBI36
NG_008690.1:g.75834_75839delinsACATTT
NG_008690.2:g.116642_116647delinsACATTT

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.969+126_969+131delinsACATTT MANE Select ENSP00000448059.1:n.969+126_969+131delins...
ENST00000307000.7:c.954+126_954+131delinsACATTT ENSP00000303500.2:n.954+126_954+131delins...
ENST00000549247.6:n.728+126_728+131delinsACATTT
ENST00000551114.2:n.631+126_631+131delinsACATTT
ENST00000553106.5:c.969+126_969+131delinsACATTT ENSP00000448059.1:n.969+126_969+131delins...
ENST00000635477.1:c.74-2338_74-2333delinsACATTT
ENST00000635528.1:n.484+126_484+131delinsACATTT
NM_000277.1:c.969+126_969+131delinsACATTT NP_000268.1:n.969+126_969+131delinsACATTT...
XM_011538422.1:c.913-2338_913-2333delinsACATTT XP_011536724.1:n.913-2338_913-2333delinsA...
NM_000277.2:c.969+126_969+131delinsACATTT NP_000268.1:n.969+126_969+131delinsACATTT...
NM_001354304.1:c.969+126_969+131delinsACATTT NP_001341233.1:n.969+126_969+131delinsACA...
NM_000277.3:c.969+126_969+131delinsACATTT MANE Select NP_000268.1:n.969+126_969+131delinsACATTT...
NM_001354304.2:c.969+126_969+131delinsACATTT NP_001341233.1:n.969+126_969+131delinsACA...