Canonical Allele Identifier: CA386294540
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103246604A>C (hg19) chr12:g.102852826A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852826A>C , CM000674.2:g.102852826A>C GRCh38
NC_000012.11:g.103246604A>C , CM000674.1:g.103246604A>C GRCh37
NC_000012.10:g.101770734A>C NCBI36
NG_008690.1:g.69777T>G
NG_008690.2:g.110585T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.831T>G MANE Select ENSP00000448059.1:p.Tyr277Ter
ENST00000307000.7:c.816T>G ENSP00000303500.2:p.Tyr272Ter
ENST00000549247.6:n.590T>G
ENST00000553106.5:c.831T>G ENSP00000448059.1:p.Tyr277Ter
NM_000277.1:c.831T>G NP_000268.1:p.Tyr277Ter
XM_011538422.1:c.831T>G XP_011536724.1:p.Tyr277Ter
NM_000277.2:c.831T>G NP_000268.1:p.Tyr277Ter
NM_001354304.1:c.831T>G NP_001341233.1:p.Tyr277Ter
NM_000277.3:c.831T>G MANE Select NP_000268.1:p.Tyr277Ter
NM_001354304.2:c.831T>G NP_001341233.1:p.Tyr277Ter
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