Canonical Allele Identifier: CA2201986648

Gene: NTHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046188C= , CM000678.2:g.2046188C=	GRCh38
NC_000016.9:g.2096189C= , CM000678.1:g.2096189C=	GRCh37
NC_000016.8:g.2036190C=	NCBI36
NG_005895.1:g.1883C= , LRG_487:g.1883C=
NG_008412.1:g.6679G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.3G=	ENSP00000498290.1:p.Lys1=
ENST00000651570.2:c.294G= MANE Select	ENSP00000498421.1:p.Lys98=
ENST00000651583.1:c.249G=	ENSP00000498821.1:p.Lys83=
ENST00000219066.5:c.318G=	ENSP00000219066.1:p.Lys106=
ENST00000561841.1:c.214G=
ENST00000562120.1:n.27G=
ENST00000566380.5:c.257G=
ENST00000568513.5:c.173+92G=
NM_002528.5:c.318G=	NP_002519.1:p.Lys106=
XM_011522505.1:c.318G=	XP_011520807.1:p.Lys106=
NM_001318193.1:c.318G=	NP_001305122.1:p.Lys106=
NM_001318194.1:c.24+92G=	NP_001305123.1:n.24+92G=
NM_002528.6:c.318G=	NP_002519.1:p.Lys106=
XM_017023253.1:c.318G=	XP_016878742.1:p.Lys106=
NM_001318193.2:c.294G=	NP_001305122.2:p.Lys98=
NM_002528.7:c.294G= MANE Select	NP_002519.2:p.Lys98=
NM_001318194.2:c.24+92G=	NP_001305123.1:n.24+92G=