Canonical Allele Identifier: CA2202016919
Gene: NTHL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2046066G= , CM000678.2:g.2046066G= GRCh38
NC_000016.9:g.2096067G= , CM000678.1:g.2096067G= GRCh37
NC_000016.8:g.2036068G= NCBI36
NG_005895.1:g.1761G= , LRG_487:g.1761G=
NG_008412.1:g.6801C=

Transcript Alleles

HGVS Amino-acid change
ENST00000651522.1:c.63+62C= ENSP00000498290.1:n.63+62C=
ENST00000651570.2:c.354+62C= MANE Select ENSP00000498421.1:n.354+62C=
ENST00000651583.1:c.309+62C= ENSP00000498821.1:n.309+62C=
ENST00000219066.5:c.378+62C= ENSP00000219066.1:n.378+62C=
ENST00000561841.1:c.274+62C=
ENST00000562120.1:n.87+62C=
ENST00000566380.5:c.317+62C=
ENST00000568513.5:c.173+214C=
NM_002528.5:c.378+62C= NP_002519.1:n.378+62C=
XM_011522505.1:c.378+62C= XP_011520807.1:n.378+62C=
NM_001318193.1:c.378+62C= NP_001305122.1:n.378+62C=
NM_001318194.1:c.24+214C= NP_001305123.1:n.24+214C=
NM_002528.6:c.378+62C= NP_002519.1:n.378+62C=
XM_017023253.1:c.378+62C= XP_016878742.1:n.378+62C=
NM_001318193.2:c.354+62C= NP_001305122.2:n.354+62C=
NM_002528.7:c.354+62C= MANE Select NP_002519.2:n.354+62C=
NM_001318194.2:c.24+214C= NP_001305123.1:n.24+214C=