Canonical Allele Identifier: CA2201986712

Gene: NTHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046224T= , CM000678.2:g.2046224T=	GRCh38
NC_000016.9:g.2096225T= , CM000678.1:g.2096225T=	GRCh37
NC_000016.8:g.2036226T=	NCBI36
NG_005895.1:g.1919T= , LRG_487:g.1919T=
NG_008412.1:g.6643A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.258A= MANE Select	ENSP00000498421.1:p.Gln86=
ENST00000651583.1:c.213A=	ENSP00000498821.1:p.Gln71=
ENST00000219066.5:c.282A=	ENSP00000219066.1:p.Gln94=
ENST00000561841.1:c.178A=
ENST00000566380.5:c.221A=
ENST00000568513.5:c.173+56A=
NM_002528.5:c.282A=	NP_002519.1:p.Gln94=
XM_011522505.1:c.282A=	XP_011520807.1:p.Gln94=
NM_001318193.1:c.282A=	NP_001305122.1:p.Gln94=
NM_001318194.1:c.24+56A=	NP_001305123.1:n.24+56A=
NM_002528.6:c.282A=	NP_002519.1:p.Gln94=
XM_017023253.1:c.282A=	XP_016878742.1:p.Gln94=
NM_001318193.2:c.258A=	NP_001305122.2:p.Gln86=
NM_002528.7:c.258A= MANE Select	NP_002519.2:p.Gln86=
NM_001318194.2:c.24+56A=	NP_001305123.1:n.24+56A=