Canonical Allele Identifier: CA346938865

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55908001G>C (hg19) ; chr2:g.55680866G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680866G>C , CM000664.2:g.55680866G>C	GRCh38
NC_000002.11:g.55908001G>C , CM000664.1:g.55908001G>C	GRCh37
NC_000002.10:g.55761505G>C	NCBI36
NG_033012.1:g.18045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.506C>G MANE Select	ENSP00000400646.2:p.Ala169Gly
ENST00000260604.8:c.506C>G	ENSP00000260604.4:p.Ala169Gly
ENST00000415374.5:c.506C>G	ENSP00000393953.1:p.Ala169Gly
ENST00000429805.1:c.*154C>G	ENSP00000411994.1:n.*154C>G
ENST00000447944.6:c.506C>G	ENSP00000400646.2:p.Ala169Gly
NM_033109.4:c.506C>G	NP_149100.2:p.Ala169Gly
XM_005264629.1:c.266C>G	XP_005264686.1:p.Ala89Gly
XM_011533142.1:c.506C>G	XP_011531444.1:p.Ala169Gly
XM_005264629.2:c.266C>G	XP_005264686.1:p.Ala89Gly
XM_017005172.1:c.266C>G	XP_016860661.1:p.Ala89Gly
XR_001739010.1:n.536C>G
NM_033109.5:c.506C>G MANE Select	NP_149100.2:p.Ala169Gly