Canonical Allele Identifier: CA426175449

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55908003T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680868T>G , CM000664.2:g.55680868T>G	GRCh38
NC_000002.11:g.55908003T>G , CM000664.1:g.55908003T>G	GRCh37
NC_000002.10:g.55761507T>G	NCBI36
NG_033012.1:g.18043A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.504A>C MANE Select	ENSP00000400646.2:p.Leu168=
ENST00000260604.8:c.504A>C	ENSP00000260604.4:p.Leu168=
ENST00000415374.5:c.504A>C	ENSP00000393953.1:p.Leu168=
ENST00000429805.1:c.*152A>C	ENSP00000411994.1:n.*152A>C
ENST00000447944.6:c.504A>C	ENSP00000400646.2:p.Leu168=
NM_033109.4:c.504A>C	NP_149100.2:p.Leu168=
XM_005264629.1:c.264A>C	XP_005264686.1:p.Leu88=
XM_011533142.1:c.504A>C	XP_011531444.1:p.Leu168=
XM_005264629.2:c.264A>C	XP_005264686.1:p.Leu88=
XM_017005172.1:c.264A>C	XP_016860661.1:p.Leu88=
XR_001739010.1:n.534A>C
NM_033109.5:c.504A>C MANE Select	NP_149100.2:p.Leu168=