Canonical Allele Identifier: CA913187280

Gene: PAH

Linked Data

• gnomAD v4: 12-102917168-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102917168G>T , CM000674.2:g.102917168G>T	GRCh38
NC_000012.11:g.103310946G>T , CM000674.1:g.103310946G>T	GRCh37
NC_000012.10:g.101835076G>T	NCBI36
NG_008690.1:g.5435C>A
NG_008690.2:g.46243C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.-38C>A MANE Select	ENSP00000448059.1:n.-38C>A
ENST00000307000.7:c.-185C>A	ENSP00000303500.2:n.-185C>A
ENST00000546844.1:c.-38C>A	ENSP00000446658.1:n.-38C>A
ENST00000547319.1:n.274C>A
ENST00000549111.5:n.59C>A
ENST00000551337.5:c.-38C>A	ENSP00000447620.1:n.-38C>A
ENST00000551988.5:n.52C>A
ENST00000553106.5:c.-38C>A	ENSP00000448059.1:n.-38C>A
ENST00000635500.1:n.29-4270C>A
NM_000277.1:c.-38C>A	NP_000268.1:n.-38C>A
XM_011538422.1:c.-38C>A	XP_011536724.1:n.-38C>A
NM_000277.2:c.-38C>A	NP_000268.1:n.-38C>A
NM_001354304.1:c.-38C>A	NP_001341233.1:n.-38C>A
XM_017019370.2:c.-38C>A	XP_016874859.1:n.-38C>A
NM_000277.3:c.-38C>A MANE Select	NP_000268.1:n.-38C>A
NM_001354304.2:c.-38C>A	NP_001341233.1:n.-38C>A