Canonical Allele Identifier: CA2620514146

Gene: PAH

Linked Data

• gnomAD v4: 12-102852673-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852673A>G , CM000674.2:g.102852673A>G	GRCh38
NC_000012.11:g.103246451A>G , CM000674.1:g.103246451A>G	GRCh37
NC_000012.10:g.101770581A>G	NCBI36
NG_008690.1:g.69930T>C
NG_008690.2:g.110738T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.842+142T>C MANE Select	ENSP00000448059.1:n.842+142T>C
ENST00000307000.7:c.827+142T>C	ENSP00000303500.2:n.827+142T>C
ENST00000549247.6:n.601+142T>C
ENST00000553106.5:c.842+142T>C	ENSP00000448059.1:n.842+142T>C
ENST00000635477.1:c.3+142T>C
NM_000277.1:c.842+142T>C	NP_000268.1:n.842+142T>C
XM_011538422.1:c.842+142T>C	XP_011536724.1:n.842+142T>C
NM_000277.2:c.842+142T>C	NP_000268.1:n.842+142T>C
NM_001354304.1:c.842+142T>C	NP_001341233.1:n.842+142T>C
NM_000277.3:c.842+142T>C MANE Select	NP_000268.1:n.842+142T>C
NM_001354304.2:c.842+142T>C	NP_001341233.1:n.842+142T>C