Canonical Allele Identifier: CA16020789
Community Standard Title: NM_000277.3(PAH):c.442G>C (p.Gly148Arg)
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866663C>G , CM000674.2:g.102866663C>G GRCh38
NC_000012.11:g.103260441C>G , CM000674.1:g.103260441C>G GRCh37
NC_000012.10:g.101784571C>G NCBI36
NG_008690.1:g.55940G>C
NG_008690.2:g.96748G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.442G>C MANE Select NP_000268.1:p.Gly148Arg
ENST00000553106.6:c.442G>C MANE Select ENSP00000448059.1:p.Gly148Arg
NM_000277.1:c.442G>C NP_000268.1:p.Gly148Arg
NM_000277.2:c.442G>C NP_000268.1:p.Gly148Arg
NM_001354304.1:c.442G>C NP_001341233.1:p.Gly148Arg
NM_001354304.2:c.442G>C NP_001341233.1:p.Gly148Arg
ENST00000307000.7:c.427G>C ENSP00000303500.2:p.Gly143Arg
ENST00000549111.5:n.538G>C
ENST00000551988.5:n.530+10799G>C
ENST00000553106.5:c.442G>C ENSP00000448059.1:p.Gly148Arg
XM_011538422.1:c.442G>C XP_011536724.1:p.Gly148Arg
XM_017019370.2:c.442G>C XP_016874859.1:p.Gly148Arg
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