Canonical Allele Identifier: CA2620514447
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852808_102852815dup , CM000674.2:g.102852808_102852815dup GRCh38
NC_000012.11:g.103246586_103246593dup , CM000674.1:g.103246586_103246593dup GRCh37
NC_000012.10:g.101770716_101770723dup NCBI36
NG_008690.1:g.69789_69796dup
NG_008690.2:g.110597_110604dup

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.842+1_842+8dup
ENST00000307000.7:c.827+1_827+8dup
ENST00000549247.6:n.601+1_601+8dup
ENST00000553106.5:c.842+1_842+8dup
ENST00000635477.1:c.3+1_3+8dup
NM_000277.1:c.842+1_842+8dup
XM_011538422.1:c.842+1_842+8dup
NM_000277.2:c.842+1_842+8dup
NM_001354304.1:c.842+1_842+8dup
NM_000277.3:c.842+1_842+8dup
NM_001354304.2:c.842+1_842+8dup