Canonical Allele Identifier: CA386296763
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855258T>A , CM000674.2:g.102855258T>A GRCh38
NC_000012.11:g.103249036T>A , CM000674.1:g.103249036T>A GRCh37
NC_000012.10:g.101773166T>A NCBI36
NG_008690.1:g.67345A>T
NG_008690.2:g.108153A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.584A>T MANE Select ENSP00000448059.1:p.Lys195Met
ENST00000307000.7:c.569A>T ENSP00000303500.2:p.Lys190Met
ENST00000549111.5:n.680A>T
ENST00000553106.5:c.584A>T ENSP00000448059.1:p.Lys195Met
NM_000277.1:c.584A>T NP_000268.1:p.Lys195Met
XM_011538422.1:c.584A>T XP_011536724.1:p.Lys195Met
NM_000277.2:c.584A>T NP_000268.1:p.Lys195Met
NM_001354304.1:c.584A>T NP_001341233.1:p.Lys195Met
XM_017019370.2:c.584A>T XP_016874859.1:p.Lys195Met
NM_000277.3:c.584A>T MANE Select NP_000268.1:p.Lys195Met
NM_001354304.2:c.584A>T NP_001341233.1:p.Lys195Met