Canonical Allele Identifier: CA1668457

Gene: PNPT1

Linked Data

• dbSNP Id: rs749022769
• ExAC: 2:55908043 T / C
• gnomAD v2: 2-55908043-T-C
• gnomAD v3: 2-55680908-T-C
• gnomAD v4: 2-55680908-T-C
• MyVariant Identifiers: chr2:g.55908043T>C (hg19) ; chr2:g.55680908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680908T>C , CM000664.2:g.55680908T>C	GRCh38
NC_000002.11:g.55908043T>C , CM000664.1:g.55908043T>C	GRCh37
NC_000002.10:g.55761547T>C	NCBI36
NG_033012.1:g.18003A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.464A>G MANE Select	ENSP00000400646.2:p.Asn155Ser
ENST00000260604.8:c.464A>G	ENSP00000260604.4:p.Asn155Ser
ENST00000415374.5:c.464A>G	ENSP00000393953.1:p.Asn155Ser
ENST00000429805.1:c.*112A>G	ENSP00000411994.1:n.*112A>G
ENST00000447944.6:c.464A>G	ENSP00000400646.2:p.Asn155Ser
NM_033109.4:c.464A>G	NP_149100.2:p.Asn155Ser
XM_005264629.1:c.224A>G	XP_005264686.1:p.Asn75Ser
XM_011533142.1:c.464A>G	XP_011531444.1:p.Asn155Ser
XM_005264629.2:c.224A>G	XP_005264686.1:p.Asn75Ser
XM_017005172.1:c.224A>G	XP_016860661.1:p.Asn75Ser
XR_001739010.1:n.494A>G
NM_033109.5:c.464A>G MANE Select	NP_149100.2:p.Asn155Ser