Canonical Allele Identifier: CA2201986583
Gene: NTHL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2046146G= , CM000678.2:g.2046146G= GRCh38
NC_000016.9:g.2096147G= , CM000678.1:g.2096147G= GRCh37
NC_000016.8:g.2036148G= NCBI36
NG_005895.1:g.1841G= , LRG_487:g.1841G=
NG_008412.1:g.6721C=

Transcript Alleles

HGVS Amino-acid change
ENST00000651522.1:c.45C= ENSP00000498290.1:p.Asp15=
ENST00000651570.2:c.336C= MANE Select ENSP00000498421.1:p.Asp112=
ENST00000651583.1:c.291C= ENSP00000498821.1:p.Asp97=
ENST00000219066.5:c.360C= ENSP00000219066.1:p.Asp120=
ENST00000561841.1:c.256C=
ENST00000562120.1:n.69C=
ENST00000566380.5:c.299C=
ENST00000568513.5:c.173+134C=
NM_002528.5:c.360C= NP_002519.1:p.Asp120=
XM_011522505.1:c.360C= XP_011520807.1:p.Asp120=
NM_001318193.1:c.360C= NP_001305122.1:p.Asp120=
NM_001318194.1:c.24+134C= NP_001305123.1:n.24+134C=
NM_002528.6:c.360C= NP_002519.1:p.Asp120=
XM_017023253.1:c.360C= XP_016878742.1:p.Asp120=
NM_001318193.2:c.336C= NP_001305122.2:p.Asp112=
NM_002528.7:c.336C= MANE Select NP_002519.2:p.Asp112=
NM_001318194.2:c.24+134C= NP_001305123.1:n.24+134C=