Canonical Allele Identifier: CA394295607
Gene: NTHL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2046192T>A , CM000678.2:g.2046192T>A GRCh38
NC_000016.9:g.2096193T>A , CM000678.1:g.2096193T>A GRCh37
NC_000016.8:g.2036194T>A NCBI36
NG_005895.1:g.1887T>A , LRG_487:g.1887T>A
NG_008412.1:g.6675A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651570.2:c.290A>T MANE Select ENSP00000498421.1:p.Lys97Ile
ENST00000651583.1:c.245A>T ENSP00000498821.1:p.Lys82Ile
ENST00000219066.5:c.314A>T ENSP00000219066.1:p.Lys105Ile
ENST00000561841.1:c.210A>T
ENST00000562120.1:n.23A>T
ENST00000566380.5:c.253A>T
ENST00000568513.5:c.173+88A>T
NM_002528.5:c.314A>T NP_002519.1:p.Lys105Ile
XM_011522505.1:c.314A>T XP_011520807.1:p.Lys105Ile
NM_001318193.1:c.314A>T NP_001305122.1:p.Lys105Ile
NM_001318194.1:c.24+88A>T NP_001305123.1:n.24+88A>T
NM_002528.6:c.314A>T NP_002519.1:p.Lys105Ile
XM_017023253.1:c.314A>T XP_016878742.1:p.Lys105Ile
NM_001318193.2:c.290A>T NP_001305122.2:p.Lys97Ile
NM_002528.7:c.290A>T MANE Select NP_002519.2:p.Lys97Ile
NM_001318194.2:c.24+88A>T NP_001305123.1:n.24+88A>T