Canonical Allele Identifier: CA3260670108
Community Standard Title: NC_000012.12:g.102866576_102866683dup
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866576_102866683dup , CM000674.2:g.102866576_102866683dup GRCh38
NC_000012.11:g.103260354_103260461dup , CM000674.1:g.103260354_103260461dup GRCh37
NC_000012.10:g.101784484_101784591dup NCBI36
NG_008690.1:g.55920_56027dup
NG_008690.2:g.96728_96835dup

Transcript Alleles

HGVS Amino-acid Change
NM_000277.1:c.442-20_509+20dup
NM_000277.2:c.442-20_509+20dup
NM_000277.3:c.442-20_509+20dup
NM_001354304.1:c.442-20_509+20dup
NM_001354304.2:c.442-20_509+20dup
ENST00000307000.7:c.427-20_494+20dup
ENST00000549111.5:n.538-20_605+20dup
ENST00000551988.5:n.530+10779_530+10886dup
ENST00000553106.5:c.442-20_509+20dup
ENST00000553106.6:c.442-20_509+20dup
XM_011538422.1:c.442-20_509+20dup
XM_017019370.2:c.442-20_509+20dup