Canonical Allele Identifier: CA2620511241

Gene: PAH

Linked Data

• gnomAD v4: 12-102917329-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102917329C>A , CM000674.2:g.102917329C>A	GRCh38
NC_000012.11:g.103311107C>A , CM000674.1:g.103311107C>A	GRCh37
NC_000012.10:g.101835237C>A	NCBI36
NG_008690.1:g.5275G>T
NG_008690.2:g.46082G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546708.5:n.493-104G>T
ENST00000546844.1:c.-95-104G>T	ENSP00000446658.1:n.-95-104G>T
ENST00000547319.1:n.217-104G>T
ENST00000551337.5:c.-95-104G>T	ENSP00000447620.1:n.-95-104G>T
ENST00000553106.5:c.-199G>T	ENSP00000448059.1:n.-199G>T
ENST00000635500.1:n.29-4431G>T
NM_000277.1:c.-198G>T	NP_000268.1:n.-198G>T
NM_000277.2:c.-199G>T	NP_000268.1:n.-199G>T
NM_001354304.1:c.-95-104G>T	NP_001341233.1:n.-95-104G>T
NM_001354304.2:c.-95-104G>T	NP_001341233.1:n.-95-104G>T