Canonical Allele Identifier: CA346926179

Gene: PNPT1

Linked Data

• COSMIC: COSM5397165
• MyVariant Identifiers: chr2:g.55874582G>A (hg19) ; chr2:g.55647447G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55647447G>A , CM000664.2:g.55647447G>A	GRCh38
NC_000002.11:g.55874582G>A , CM000664.1:g.55874582G>A	GRCh37
NC_000002.10:g.55728086G>A	NCBI36
NG_033012.1:g.51464C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.1502C>T MANE Select	ENSP00000400646.2:p.Pro501Leu
ENST00000260604.8:c.*1057C>T	ENSP00000260604.4:n.*1057C>T
ENST00000415374.5:c.1502C>T	ENSP00000393953.1:p.Pro501Leu
ENST00000415489.1:c.509C>T
ENST00000447944.6:c.1502C>T	ENSP00000400646.2:p.Pro501Leu
NM_033109.4:c.1502C>T	NP_149100.2:p.Pro501Leu
XM_005264629.1:c.1262C>T	XP_005264686.1:p.Pro421Leu
XM_011533142.1:c.*34C>T	XP_011531444.1:n.*34C>T
XM_005264629.2:c.1262C>T	XP_005264686.1:p.Pro421Leu
XM_017005172.1:c.1262C>T	XP_016860661.1:p.Pro421Leu
XR_001739010.1:n.1579C>T
NM_033109.5:c.1502C>T MANE Select	NP_149100.2:p.Pro501Leu