Canonical Allele Identifier: CA2620507155
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102877395-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877397del , CM000674.2:g.102877397del GRCh38
NC_000012.11:g.103271175del , CM000674.1:g.103271175del GRCh37
NC_000012.10:g.101795305del NCBI36
NG_008690.1:g.45207del
NG_008690.2:g.86015del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.441+66del MANE Select ENSP00000448059.1:n.441+66del
ENST00000307000.7:c.426+66del ENSP00000303500.2:n.426+66del
ENST00000549111.5:n.537+66del
ENST00000550978.6:c.491del
ENST00000551988.5:n.530+66del
ENST00000553106.5:c.441+66del ENSP00000448059.1:n.441+66del
NM_000277.1:c.441+66del NP_000268.1:n.441+66del
XM_011538422.1:c.441+66del XP_011536724.1:n.441+66del
NM_000277.2:c.441+66del NP_000268.1:n.441+66del
NM_001354304.1:c.441+66del NP_001341233.1:n.441+66del
XM_017019370.2:c.441+66del XP_016874859.1:n.441+66del
NM_000277.3:c.441+66del MANE Select NP_000268.1:n.441+66del
NM_001354304.2:c.441+66del NP_001341233.1:n.441+66del
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