Canonical Allele Identifier: CA386302554

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103306631A>G (hg19) ; chr12:g.102912853A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912853A>G , CM000674.2:g.102912853A>G	GRCh38
NC_000012.11:g.103306631A>G , CM000674.1:g.103306631A>G	GRCh37
NC_000012.10:g.101830761A>G	NCBI36
NG_008690.1:g.9750T>C
NG_008690.2:g.50558T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.106T>C MANE Select	ENSP00000448059.1:p.Ser36Pro
ENST00000307000.7:c.91T>C	ENSP00000303500.2:p.Ser31Pro
ENST00000546844.1:c.106T>C	ENSP00000446658.1:p.Ser36Pro
ENST00000548677.2:n.193T>C
ENST00000548928.1:n.28T>C
ENST00000549111.5:n.202T>C
ENST00000550978.6:c.90T>C
ENST00000551337.5:c.106T>C	ENSP00000447620.1:p.Ser36Pro
ENST00000551988.5:n.195T>C
ENST00000553106.5:c.106T>C	ENSP00000448059.1:p.Ser36Pro
ENST00000635500.1:n.74T>C
NM_000277.1:c.106T>C	NP_000268.1:p.Ser36Pro
XM_011538422.1:c.106T>C	XP_011536724.1:p.Ser36Pro
NM_000277.2:c.106T>C	NP_000268.1:p.Ser36Pro
NM_001354304.1:c.106T>C	NP_001341233.1:p.Ser36Pro
XM_017019370.2:c.106T>C	XP_016874859.1:p.Ser36Pro
NM_000277.3:c.106T>C MANE Select	NP_000268.1:p.Ser36Pro
NM_001354304.2:c.106T>C	NP_001341233.1:p.Ser36Pro