Canonical Allele Identifier: CA386304086

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103288594G>C (hg19) ; chr12:g.102894816G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102894816G>C , CM000674.2:g.102894816G>C	GRCh38
NC_000012.11:g.103288594G>C , CM000674.1:g.103288594G>C	GRCh37
NC_000012.10:g.101812724G>C	NCBI36
NG_008690.1:g.27787C>G
NG_008690.2:g.68595C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.271C>G MANE Select	ENSP00000448059.1:p.Leu91Val
ENST00000307000.7:c.256C>G	ENSP00000303500.2:p.Leu86Val
ENST00000546844.1:c.271C>G	ENSP00000446658.1:p.Leu91Val
ENST00000548677.2:n.358C>G
ENST00000548928.1:n.193C>G
ENST00000549111.5:n.367C>G
ENST00000550978.6:c.255C>G
ENST00000551337.5:c.271C>G	ENSP00000447620.1:p.Leu91Val
ENST00000551988.5:n.360C>G
ENST00000553106.5:c.271C>G	ENSP00000448059.1:p.Leu91Val
NM_000277.1:c.271C>G	NP_000268.1:p.Leu91Val
XM_011538422.1:c.271C>G	XP_011536724.1:p.Leu91Val
NM_000277.2:c.271C>G	NP_000268.1:p.Leu91Val
NM_001354304.1:c.271C>G	NP_001341233.1:p.Leu91Val
XM_017019370.2:c.271C>G	XP_016874859.1:p.Leu91Val
NM_000277.3:c.271C>G MANE Select	NP_000268.1:p.Leu91Val
NM_001354304.2:c.271C>G	NP_001341233.1:p.Leu91Val