Canonical Allele Identifier: CA2201986707

Gene: NTHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046223G= , CM000678.2:g.2046223G=	GRCh38
NC_000016.9:g.2096224G= , CM000678.1:g.2096224G=	GRCh37
NC_000016.8:g.2036225G=	NCBI36
NG_005895.1:g.1918G= , LRG_487:g.1918G=
NG_008412.1:g.6644C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.259C= MANE Select	ENSP00000498421.1:p.Gln87=
ENST00000651583.1:c.214C=	ENSP00000498821.1:p.Gln72=
ENST00000219066.5:c.283C=	ENSP00000219066.1:p.Gln95=
ENST00000561841.1:c.179C=
ENST00000566380.5:c.222C=
ENST00000568513.5:c.173+57C=
NM_002528.5:c.283C=	NP_002519.1:p.Gln95=
XM_011522505.1:c.283C=	XP_011520807.1:p.Gln95=
NM_001318193.1:c.283C=	NP_001305122.1:p.Gln95=
NM_001318194.1:c.24+57C=	NP_001305123.1:n.24+57C=
NM_002528.6:c.283C=	NP_002519.1:p.Gln95=
XM_017023253.1:c.283C=	XP_016878742.1:p.Gln95=
NM_001318193.2:c.259C=	NP_001305122.2:p.Gln87=
NM_002528.7:c.259C= MANE Select	NP_002519.2:p.Gln87=
NM_001318194.2:c.24+57C=	NP_001305123.1:n.24+57C=