Canonical Allele Identifier: CA1252405791

Gene: PNPT1

Linked Data

• dbSNP Id: rs1697232233

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55681086A>G , CM000664.2:g.55681086A>G	GRCh38
NC_000002.11:g.55908221A>G , CM000664.1:g.55908221A>G	GRCh37
NC_000002.10:g.55761725A>G	NCBI36
NG_033012.1:g.17825T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.454-168T>C MANE Select	ENSP00000400646.2:n.454-168T>C
ENST00000260604.8:c.454-168T>C	ENSP00000260604.4:n.454-168T>C
ENST00000415374.5:c.454-168T>C	ENSP00000393953.1:n.454-168T>C
ENST00000429805.1:c.*102-168T>C	ENSP00000411994.1:n.*102-168T>C
ENST00000447944.6:c.454-168T>C	ENSP00000400646.2:n.454-168T>C
NM_033109.4:c.454-168T>C	NP_149100.2:n.454-168T>C
XM_005264629.1:c.214-168T>C	XP_005264686.1:n.214-168T>C
XM_011533142.1:c.454-168T>C	XP_011531444.1:n.454-168T>C
XM_005264629.2:c.214-168T>C	XP_005264686.1:n.214-168T>C
XM_017005172.1:c.214-168T>C	XP_016860661.1:n.214-168T>C
XR_001739010.1:n.484-168T>C
NM_033109.5:c.454-168T>C MANE Select	NP_149100.2:n.454-168T>C