Canonical Allele Identifier: CA2797244100
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917303G>C , CM000674.2:g.102917303G>C GRCh38
NC_000012.11:g.103311081G>C , CM000674.1:g.103311081G>C GRCh37
NC_000012.10:g.101835211G>C NCBI36
NG_008690.1:g.5301C>G
NG_008690.2:g.46108C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-78C>G
ENST00000546844.1:c.-95-78C>G ENSP00000446658.1:n.-95-78C>G
ENST00000547319.1:n.217-78C>G
ENST00000551337.5:c.-95-78C>G ENSP00000447620.1:n.-95-78C>G
ENST00000553106.5:c.-173C>G ENSP00000448059.1:n.-173C>G
ENST00000635500.1:n.29-4405C>G
NM_000277.1:c.-172C>G NP_000268.1:n.-172C>G
NM_000277.2:c.-173C>G NP_000268.1:n.-173C>G
NM_001354304.1:c.-95-78C>G NP_001341233.1:n.-95-78C>G
NM_001354304.2:c.-95-78C>G NP_001341233.1:n.-95-78C>G