Canonical Allele Identifier: CA2202016928

Gene: NTHL1

Linked Data

• dbSNP Id: rs2084357854

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046087T>G , CM000678.2:g.2046087T>G	GRCh38
NC_000016.9:g.2096088T>G , CM000678.1:g.2096088T>G	GRCh37
NC_000016.8:g.2036089T>G	NCBI36
NG_005895.1:g.1782T>G , LRG_487:g.1782T>G
NG_008412.1:g.6780A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.63+41A>C	ENSP00000498290.1:n.63+41A>C
ENST00000651570.2:c.354+41A>C MANE Select	ENSP00000498421.1:n.354+41A>C
ENST00000651583.1:c.309+41A>C	ENSP00000498821.1:n.309+41A>C
ENST00000219066.5:c.378+41A>C	ENSP00000219066.1:n.378+41A>C
ENST00000561841.1:c.274+41A>C
ENST00000562120.1:n.87+41A>C
ENST00000566380.5:c.317+41A>C
ENST00000568513.5:c.173+193A>C
NM_002528.5:c.378+41A>C	NP_002519.1:n.378+41A>C
XM_011522505.1:c.378+41A>C	XP_011520807.1:n.378+41A>C
NM_001318193.1:c.378+41A>C	NP_001305122.1:n.378+41A>C
NM_001318194.1:c.24+193A>C	NP_001305123.1:n.24+193A>C
NM_002528.6:c.378+41A>C	NP_002519.1:n.378+41A>C
XM_017023253.1:c.378+41A>C	XP_016878742.1:n.378+41A>C
NM_001318193.2:c.354+41A>C	NP_001305122.2:n.354+41A>C
NM_002528.7:c.354+41A>C MANE Select	NP_002519.2:n.354+41A>C
NM_001318194.2:c.24+193A>C	NP_001305123.1:n.24+193A>C