Canonical Allele Identifier: CA2201986620

Gene: NTHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046174T= , CM000678.2:g.2046174T=	GRCh38
NC_000016.9:g.2096175T= , CM000678.1:g.2096175T=	GRCh37
NC_000016.8:g.2036176T=	NCBI36
NG_005895.1:g.1869T= , LRG_487:g.1869T=
NG_008412.1:g.6693A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.17A=	ENSP00000498290.1:p.Asp6=
ENST00000651570.2:c.308A= MANE Select	ENSP00000498421.1:p.Asp103=
ENST00000651583.1:c.263A=	ENSP00000498821.1:p.Asp88=
ENST00000219066.5:c.332A=	ENSP00000219066.1:p.Asp111=
ENST00000561841.1:c.228A=
ENST00000562120.1:n.41A=
ENST00000566380.5:c.271A=
ENST00000568513.5:c.173+106A=
NM_002528.5:c.332A=	NP_002519.1:p.Asp111=
XM_011522505.1:c.332A=	XP_011520807.1:p.Asp111=
NM_001318193.1:c.332A=	NP_001305122.1:p.Asp111=
NM_001318194.1:c.24+106A=	NP_001305123.1:n.24+106A=
NM_002528.6:c.332A=	NP_002519.1:p.Asp111=
XM_017023253.1:c.332A=	XP_016878742.1:p.Asp111=
NM_001318193.2:c.308A=	NP_001305122.2:p.Asp103=
NM_002528.7:c.308A= MANE Select	NP_002519.2:p.Asp103=
NM_001318194.2:c.24+106A=	NP_001305123.1:n.24+106A=