Canonical Allele Identifier: CA2697551521
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2751645
ClinVar RCV Id: RCV003495702

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855290_102855292del , CM000674.2:g.102855290_102855292del GRCh38
NC_000012.11:g.103249068_103249070del , CM000674.1:g.103249068_103249070del GRCh37
NC_000012.10:g.101773198_101773200del NCBI36
NG_008690.1:g.67313_67315del
NG_008690.2:g.108121_108123del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.552_554del MANE Select ENSP00000448059.1:p.Lys185del
ENST00000307000.7:c.537_539del ENSP00000303500.2:p.Lys180del
ENST00000549111.5:n.648_650del
ENST00000551988.5:n.573_575del
ENST00000553106.5:c.552_554del ENSP00000448059.1:p.Lys185del
NM_000277.1:c.552_554del NP_000268.1:p.Lys185del
XM_011538422.1:c.552_554del XP_011536724.1:p.Lys185del
NM_000277.2:c.552_554del NP_000268.1:p.Lys185del
NM_001354304.1:c.552_554del NP_001341233.1:p.Lys185del
XM_017019370.2:c.552_554del XP_016874859.1:p.Lys185del
NM_000277.3:c.552_554del MANE Select NP_000268.1:p.Lys185del
NM_001354304.2:c.552_554del NP_001341233.1:p.Lys185del