Canonical Allele Identifier: CA47661892

Gene: PNPT1

Linked Data

• dbSNP Id: rs939750574
• gnomAD v2: 2-55894077-T-A
• gnomAD v3: 2-55666942-T-A
• gnomAD v4: 2-55666942-T-A
• MyVariant Identifiers: chr2:g.55894077T>A (hg19) ; chr2:g.55666942T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55666942T>A , CM000664.2:g.55666942T>A	GRCh38
NC_000002.11:g.55894077T>A , CM000664.1:g.55894077T>A	GRCh37
NC_000002.10:g.55747581T>A	NCBI36
NG_033012.1:g.31969A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.1176+49A>T MANE Select	ENSP00000400646.2:n.1176+49A>T
ENST00000260604.8:c.*731+49A>T	ENSP00000260604.4:n.*731+49A>T
ENST00000415374.5:c.1176+49A>T	ENSP00000393953.1:n.1176+49A>T
ENST00000415489.1:c.250+49A>T
ENST00000447944.6:c.1176+49A>T	ENSP00000400646.2:n.1176+49A>T
NM_033109.4:c.1176+49A>T	NP_149100.2:n.1176+49A>T
XM_005264629.1:c.936+49A>T	XP_005264686.1:n.936+49A>T
XM_011533142.1:c.1176+49A>T	XP_011531444.1:n.1176+49A>T
XM_005264629.2:c.936+49A>T	XP_005264686.1:n.936+49A>T
XM_017005172.1:c.936+49A>T	XP_016860661.1:n.936+49A>T
XR_001739010.1:n.1206+49A>T
NM_033109.5:c.1176+49A>T MANE Select	NP_149100.2:n.1176+49A>T