Canonical Allele Identifier: CA951242343
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1874670587
gnomAD v3: 12-102843368-CT-C
gnomAD v4: 12-102843368-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843370del , CM000674.2:g.102843370del GRCh38
NC_000012.11:g.103237148del , CM000674.1:g.103237148del GRCh37
NC_000012.10:g.101761278del NCBI36
NG_008690.1:g.79234del
NG_008690.2:g.120042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1199+277del MANE Select ENSP00000448059.1:n.1199+277del
ENST00000307000.7:c.1184+277del ENSP00000303500.2:n.1184+277del
ENST00000549247.6:n.958+277del
ENST00000551114.2:n.861+277del
ENST00000553106.5:c.1199+277del ENSP00000448059.1:n.1199+277del
ENST00000635477.1:c.303+277del
ENST00000635528.1:n.714+277del
NM_000277.1:c.1199+277del NP_000268.1:n.1199+277del
XM_011538422.1:c.1142+277del XP_011536724.1:n.1142+277del
NM_000277.2:c.1199+277del NP_000268.1:n.1199+277del
NM_001354304.1:c.1199+277del NP_001341233.1:n.1199+277del
NM_000277.3:c.1199+277del MANE Select NP_000268.1:n.1199+277del
NM_001354304.2:c.1199+277del NP_001341233.1:n.1199+277del
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