Canonical Allele Identifier: CA2620511188
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917318G>C , CM000674.2:g.102917318G>C GRCh38
NC_000012.11:g.103311096G>C , CM000674.1:g.103311096G>C GRCh37
NC_000012.10:g.101835226G>C NCBI36
NG_008690.1:g.5286C>G
NG_008690.2:g.46093C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-93C>G
ENST00000546844.1:c.-95-93C>G ENSP00000446658.1:n.-95-93C>G
ENST00000547319.1:n.217-93C>G
ENST00000551337.5:c.-95-93C>G ENSP00000447620.1:n.-95-93C>G
ENST00000553106.5:c.-188C>G ENSP00000448059.1:n.-188C>G
ENST00000635500.1:n.29-4420C>G
NM_000277.1:c.-187C>G NP_000268.1:n.-187C>G
NM_000277.2:c.-188C>G NP_000268.1:n.-188C>G
NM_001354304.1:c.-95-93C>G NP_001341233.1:n.-95-93C>G
NM_001354304.2:c.-95-93C>G NP_001341233.1:n.-95-93C>G