Canonical Allele Identifier: CA2620514177

Gene: PAH

Linked Data

• gnomAD v4: 12-102852686-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852686A>T , CM000674.2:g.102852686A>T	GRCh38
NC_000012.11:g.103246464A>T , CM000674.1:g.103246464A>T	GRCh37
NC_000012.10:g.101770594A>T	NCBI36
NG_008690.1:g.69917T>A
NG_008690.2:g.110725T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.842+129T>A MANE Select	ENSP00000448059.1:n.842+129T>A
ENST00000307000.7:c.827+129T>A	ENSP00000303500.2:n.827+129T>A
ENST00000549247.6:n.601+129T>A
ENST00000553106.5:c.842+129T>A	ENSP00000448059.1:n.842+129T>A
ENST00000635477.1:c.3+129T>A
NM_000277.1:c.842+129T>A	NP_000268.1:n.842+129T>A
XM_011538422.1:c.842+129T>A	XP_011536724.1:n.842+129T>A
NM_000277.2:c.842+129T>A	NP_000268.1:n.842+129T>A
NM_001354304.1:c.842+129T>A	NP_001341233.1:n.842+129T>A
NM_000277.3:c.842+129T>A MANE Select	NP_000268.1:n.842+129T>A
NM_001354304.2:c.842+129T>A	NP_001341233.1:n.842+129T>A