Canonical Allele Identifier: CA770363165

Gene: PNPT1

Linked Data

• dbSNP Id: rs1320483450
• gnomAD v3: 2-55681170-G-A
• gnomAD v4: 2-55681170-G-A
• MyVariant Identifiers: chr2:g.55908305G>A (hg19) ; chr2:g.55681170G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55681170G>A , CM000664.2:g.55681170G>A	GRCh38
NC_000002.11:g.55908305G>A , CM000664.1:g.55908305G>A	GRCh37
NC_000002.10:g.55761809G>A	NCBI36
NG_033012.1:g.17741C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.454-252C>T MANE Select	ENSP00000400646.2:n.454-252C>T
ENST00000260604.8:c.454-252C>T	ENSP00000260604.4:n.454-252C>T
ENST00000415374.5:c.454-252C>T	ENSP00000393953.1:n.454-252C>T
ENST00000429805.1:c.*102-252C>T	ENSP00000411994.1:n.*102-252C>T
ENST00000447944.6:c.454-252C>T	ENSP00000400646.2:n.454-252C>T
NM_033109.4:c.454-252C>T	NP_149100.2:n.454-252C>T
XM_005264629.1:c.214-252C>T	XP_005264686.1:n.214-252C>T
XM_011533142.1:c.454-252C>T	XP_011531444.1:n.454-252C>T
XM_005264629.2:c.214-252C>T	XP_005264686.1:n.214-252C>T
XM_017005172.1:c.214-252C>T	XP_016860661.1:n.214-252C>T
XR_001739010.1:n.484-252C>T
NM_033109.5:c.454-252C>T MANE Select	NP_149100.2:n.454-252C>T