Canonical Allele Identifier: CA346938844

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55907990C>A (hg19) ; chr2:g.55680855C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680855C>A , CM000664.2:g.55680855C>A	GRCh38
NC_000002.11:g.55907990C>A , CM000664.1:g.55907990C>A	GRCh37
NC_000002.10:g.55761494C>A	NCBI36
NG_033012.1:g.18056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.517G>T MANE Select	ENSP00000400646.2:p.Ala173Ser
ENST00000260604.8:c.517G>T	ENSP00000260604.4:p.Gly173Cys
ENST00000415374.5:c.517G>T	ENSP00000393953.1:p.Ala173Ser
ENST00000429805.1:c.*165G>T	ENSP00000411994.1:n.*165G>T
ENST00000447944.6:c.517G>T	ENSP00000400646.2:p.Ala173Ser
NM_033109.4:c.517G>T	NP_149100.2:p.Ala173Ser
XM_005264629.1:c.277G>T	XP_005264686.1:p.Ala93Ser
XM_011533142.1:c.517G>T	XP_011531444.1:p.Ala173Ser
XM_005264629.2:c.277G>T	XP_005264686.1:p.Ala93Ser
XM_017005172.1:c.277G>T	XP_016860661.1:p.Ala93Ser
XR_001739010.1:n.547G>T
NM_033109.5:c.517G>T MANE Select	NP_149100.2:p.Ala173Ser