Canonical Allele Identifier: CA386295268

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103246631G>C (hg19) ; chr12:g.102852853G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852853G>C , CM000674.2:g.102852853G>C	GRCh38
NC_000012.11:g.103246631G>C , CM000674.1:g.103246631G>C	GRCh37
NC_000012.10:g.101770761G>C	NCBI36
NG_008690.1:g.69750C>G
NG_008690.2:g.110558C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.804C>G MANE Select	ENSP00000448059.1:p.Tyr268Ter
ENST00000307000.7:c.789C>G	ENSP00000303500.2:p.Tyr263Ter
ENST00000549247.6:n.563C>G
ENST00000553106.5:c.804C>G	ENSP00000448059.1:p.Tyr268Ter
NM_000277.1:c.804C>G	NP_000268.1:p.Tyr268Ter
XM_011538422.1:c.804C>G	XP_011536724.1:p.Tyr268Ter
NM_000277.2:c.804C>G	NP_000268.1:p.Tyr268Ter
NM_001354304.1:c.804C>G	NP_001341233.1:p.Tyr268Ter
NM_000277.3:c.804C>G MANE Select	NP_000268.1:p.Tyr268Ter
NM_001354304.2:c.804C>G	NP_001341233.1:p.Tyr268Ter