Canonical Allele Identifier: CA492953187

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096138G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046137G>C , CM000678.2:g.2046137G>C	GRCh38
NC_000016.9:g.2096138G>C , CM000678.1:g.2096138G>C	GRCh37
NC_000016.8:g.2036139G>C	NCBI36
NG_005895.1:g.1832G>C , LRG_487:g.1832G>C
NG_008412.1:g.6730C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.54C>G	ENSP00000498290.1:p.Ala18=
ENST00000651570.2:c.345C>G MANE Select	ENSP00000498421.1:p.Ala115=
ENST00000651583.1:c.300C>G	ENSP00000498821.1:p.Ala100=
ENST00000219066.5:c.369C>G	ENSP00000219066.1:p.Ala123=
ENST00000561841.1:c.265C>G
ENST00000562120.1:n.78C>G
ENST00000566380.5:c.308C>G
ENST00000568513.5:c.173+143C>G
NM_002528.5:c.369C>G	NP_002519.1:p.Ala123=
XM_011522505.1:c.369C>G	XP_011520807.1:p.Ala123=
NM_001318193.1:c.369C>G	NP_001305122.1:p.Ala123=
NM_001318194.1:c.24+143C>G	NP_001305123.1:n.24+143C>G
NM_002528.6:c.369C>G	NP_002519.1:p.Ala123=
XM_017023253.1:c.369C>G	XP_016878742.1:p.Ala123=
NM_001318193.2:c.345C>G	NP_001305122.2:p.Ala115=
NM_002528.7:c.345C>G MANE Select	NP_002519.2:p.Ala115=
NM_001318194.2:c.24+143C>G	NP_001305123.1:n.24+143C>G