Canonical Allele Identifier: CA2059476267
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1878424489

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917291del , CM000674.2:g.102917291del GRCh38
NC_000012.11:g.103311069del , CM000674.1:g.103311069del GRCh37
NC_000012.10:g.101835199del NCBI36
NG_008690.1:g.5315del
NG_008690.2:g.46123del

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-63del
ENST00000546844.1:c.-95-63del ENSP00000446658.1:n.-95-63del
ENST00000547319.1:n.217-63del
ENST00000551337.5:c.-95-63del ENSP00000447620.1:n.-95-63del
ENST00000553106.5:c.-158del ENSP00000448059.1:n.-158del
ENST00000635500.1:n.29-4390del
NM_000277.1:c.-158del NP_000268.1:n.-158del
NM_000277.2:c.-158del NP_000268.1:n.-158del
NM_001354304.1:c.-95-63del NP_001341233.1:n.-95-63del
NM_001354304.2:c.-95-63del NP_001341233.1:n.-95-63del