Canonical Allele Identifier: CA386493005
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103234222A>C (hg19) chr12:g.102840444A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840444A>C , CM000674.2:g.102840444A>C GRCh38
NC_000012.11:g.103234222A>C , CM000674.1:g.103234222A>C GRCh37
NC_000012.10:g.101758352A>C NCBI36
NG_008690.1:g.82159T>G
NG_008690.2:g.122967T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1271T>G MANE Select ENSP00000448059.1:p.Leu424Trp
ENST00000307000.7:c.1256T>G ENSP00000303500.2:p.Leu419Trp
ENST00000551114.2:n.933T>G
ENST00000553106.5:c.1271T>G ENSP00000448059.1:p.Leu424Trp
ENST00000635477.1:c.375T>G
ENST00000635528.1:n.786T>G
NM_000277.1:c.1271T>G NP_000268.1:p.Leu424Trp
XM_011538422.1:c.1214T>G XP_011536724.1:p.Leu405Trp
NM_000277.2:c.1271T>G NP_000268.1:p.Leu424Trp
NM_001354304.1:c.1271T>G NP_001341233.1:p.Leu424Trp
NM_000277.3:c.1271T>G MANE Select NP_000268.1:p.Leu424Trp
NM_001354304.2:c.1271T>G NP_001341233.1:p.Leu424Trp
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