Canonical Allele Identifier: CA492953221

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096159C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046158C>T , CM000678.2:g.2046158C>T	GRCh38
NC_000016.9:g.2096159C>T , CM000678.1:g.2096159C>T	GRCh37
NC_000016.8:g.2036160C>T	NCBI36
NG_005895.1:g.1853C>T , LRG_487:g.1853C>T
NG_008412.1:g.6709G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000651522.1:c.33G>A	ENSP00000498290.1:p.Glu11=
ENST00000651570.2:c.324G>A MANE Select	ENSP00000498421.1:p.Glu108=
ENST00000651583.1:c.279G>A	ENSP00000498821.1:p.Glu93=
ENST00000219066.5:c.348G>A	ENSP00000219066.1:p.Glu116=
ENST00000561841.1:c.244G>A
ENST00000562120.1:n.57G>A
ENST00000566380.5:c.287G>A
ENST00000568513.5:c.173+122G>A
NM_002528.5:c.348G>A	NP_002519.1:p.Glu116=
XM_011522505.1:c.348G>A	XP_011520807.1:p.Glu116=
NM_001318193.1:c.348G>A	NP_001305122.1:p.Glu116=
NM_001318194.1:c.24+122G>A	NP_001305123.1:n.24+122G>A
NM_002528.6:c.348G>A	NP_002519.1:p.Glu116=
XM_017023253.1:c.348G>A	XP_016878742.1:p.Glu116=
NM_001318193.2:c.324G>A	NP_001305122.2:p.Glu108=
NM_002528.7:c.324G>A MANE Select	NP_002519.2:p.Glu108=
NM_001318194.2:c.24+122G>A	NP_001305123.1:n.24+122G>A