Canonical Allele Identifier: CA386291550

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103240682C>A (hg19) ; chr12:g.102846904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102846904C>A , CM000674.2:g.102846904C>A	GRCh38
NC_000012.11:g.103240682C>A , CM000674.1:g.103240682C>A	GRCh37
NC_000012.10:g.101764812C>A	NCBI36
NG_008690.1:g.75699G>T
NG_008690.2:g.116507G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.960G>T MANE Select	ENSP00000448059.1:p.Lys320Asn
ENST00000307000.7:c.945G>T	ENSP00000303500.2:p.Lys315Asn
ENST00000549247.6:n.719G>T
ENST00000551114.2:n.622G>T
ENST00000553106.5:c.960G>T	ENSP00000448059.1:p.Lys320Asn
ENST00000635477.1:c.74-2473G>T
ENST00000635528.1:n.475G>T
NM_000277.1:c.960G>T	NP_000268.1:p.Lys320Asn
XM_011538422.1:c.913-2473G>T	XP_011536724.1:n.913-2473G>T
NM_000277.2:c.960G>T	NP_000268.1:p.Lys320Asn
NM_001354304.1:c.960G>T	NP_001341233.1:p.Lys320Asn
NM_000277.3:c.960G>T MANE Select	NP_000268.1:p.Lys320Asn
NM_001354304.2:c.960G>T	NP_001341233.1:p.Lys320Asn