Canonical Allele Identifier: CA1668096

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55656215G>A , CM000664.2:g.55656215G>A	GRCh38
NC_000002.11:g.55883350G>A , CM000664.1:g.55883350G>A	GRCh37
NC_000002.10:g.55736854G>A	NCBI36
NG_033012.1:g.42696C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_033109.5:c.1357C>T MANE Select	NP_149100.2:p.Leu453Phe
ENST00000447944.7:c.1357C>T MANE Select	ENSP00000400646.2:p.Leu453Phe
NM_033109.4:c.1357C>T	NP_149100.2:p.Leu453Phe
ENST00000260604.8:c.*912C>T	ENSP00000260604.4:n.*912C>T
ENST00000415374.5:c.1357C>T	ENSP00000393953.1:p.Leu453Phe
ENST00000415489.1:c.364C>T
ENST00000447944.6:c.1357C>T	ENSP00000400646.2:p.Leu453Phe
XM_005264629.1:c.1117C>T	XP_005264686.1:p.Leu373Phe
XM_005264629.2:c.1117C>T	XP_005264686.1:p.Leu373Phe
XM_011533142.1:c.1357C>T	XP_011531444.1:p.Leu453Phe
XM_017005172.1:c.1117C>T	XP_016860661.1:p.Leu373Phe
XR_001739010.1:n.1387C>T