Canonical Allele Identifier: CA2059462518
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877565_102877566delinsAG , CM000674.2:g.102877565_102877566delinsAG GRCh38
NC_000012.11:g.103271343_103271344delinsAG , CM000674.1:g.103271343_103271344delinsAG GRCh37
NC_000012.10:g.101795473_101795474delinsAG NCBI36
NG_008690.1:g.45037_45038delinsCT
NG_008690.2:g.85845_85846delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.353-16_353-15delinsCT MANE Select ENSP00000448059.1:n.353-16_353-15delinsCT...
ENST00000307000.7:c.338-16_338-15delinsCT ENSP00000303500.2:n.338-16_338-15delinsCT...
ENST00000549111.5:n.449-16_449-15delinsCT
ENST00000550978.6:c.337-16_337-15delinsCT
ENST00000551337.5:c.353-16_353-15delinsCT ENSP00000447620.1:n.353-16_353-15delinsCT...
ENST00000551988.5:n.442-16_442-15delinsCT
ENST00000553106.5:c.353-16_353-15delinsCT ENSP00000448059.1:n.353-16_353-15delinsCT...
NM_000277.1:c.353-16_353-15delinsCT NP_000268.1:n.353-16_353-15delinsCT
XM_011538422.1:c.353-16_353-15delinsCT XP_011536724.1:n.353-16_353-15delinsCT
NM_000277.2:c.353-16_353-15delinsCT NP_000268.1:n.353-16_353-15delinsCT
NM_001354304.1:c.353-16_353-15delinsCT NP_001341233.1:n.353-16_353-15delinsCT
XM_017019370.2:c.353-16_353-15delinsCT XP_016874859.1:n.353-16_353-15delinsCT
NM_000277.3:c.353-16_353-15delinsCT MANE Select NP_000268.1:n.353-16_353-15delinsCT
NM_001354304.2:c.353-16_353-15delinsCT NP_001341233.1:n.353-16_353-15delinsCT