Canonical Allele Identifier: CA386295529
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103246663G>T (hg19) chr12:g.102852885G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852885G>T , CM000674.2:g.102852885G>T GRCh38
NC_000012.11:g.103246663G>T , CM000674.1:g.103246663G>T GRCh37
NC_000012.10:g.101770793G>T NCBI36
NG_008690.1:g.69718C>A
NG_008690.2:g.110526C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.772C>A MANE Select ENSP00000448059.1:p.Leu258Met
ENST00000307000.7:c.757C>A ENSP00000303500.2:p.Leu253Met
ENST00000549247.6:n.531C>A
ENST00000553106.5:c.772C>A ENSP00000448059.1:p.Leu258Met
NM_000277.1:c.772C>A NP_000268.1:p.Leu258Met
XM_011538422.1:c.772C>A XP_011536724.1:p.Leu258Met
NM_000277.2:c.772C>A NP_000268.1:p.Leu258Met
NM_001354304.1:c.772C>A NP_001341233.1:p.Leu258Met
NM_000277.3:c.772C>A MANE Select NP_000268.1:p.Leu258Met
NM_001354304.2:c.772C>A NP_001341233.1:p.Leu258Met
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