Canonical Allele Identifier: CA346927019

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55883292A>G (hg19) ; chr2:g.55656157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55656157A>G , CM000664.2:g.55656157A>G	GRCh38
NC_000002.11:g.55883292A>G , CM000664.1:g.55883292A>G	GRCh37
NC_000002.10:g.55736796A>G	NCBI36
NG_033012.1:g.42754T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000447944.7:c.1415T>C MANE Select	ENSP00000400646.2:p.Val472Ala
ENST00000260604.8:c.*970T>C	ENSP00000260604.4:n.*970T>C
ENST00000415374.5:c.1415T>C	ENSP00000393953.1:p.Val472Ala
ENST00000415489.1:c.422T>C
ENST00000447944.6:c.1415T>C	ENSP00000400646.2:p.Val472Ala
NM_033109.4:c.1415T>C	NP_149100.2:p.Val472Ala
XM_005264629.1:c.1175T>C	XP_005264686.1:p.Val392Ala
XM_011533142.1:c.1415T>C	XP_011531444.1:p.Val472Ala
XM_005264629.2:c.1175T>C	XP_005264686.1:p.Val392Ala
XM_017005172.1:c.1175T>C	XP_016860661.1:p.Val392Ala
XR_001739010.1:n.1445T>C
NM_033109.5:c.1415T>C MANE Select	NP_149100.2:p.Val472Ala