Canonical Allele Identifier: CA394297172

Gene: NTHL1

Linked Data

• ClinVar Variation Id: 2586100
• ClinVar RCV Id: RCV003368206
• dbSNP Id: rs2150946211
• MyVariant Identifiers: chr16:g.2096238T>C (hg19) ; chr16:g.2046237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046237T>C , CM000678.2:g.2046237T>C	GRCh38
NC_000016.9:g.2096238T>C , CM000678.1:g.2096238T>C	GRCh37
NC_000016.8:g.2036239T>C	NCBI36
NG_005895.1:g.1932T>C , LRG_487:g.1932T>C
NG_008412.1:g.6630A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.245A>G MANE Select	ENSP00000498421.1:p.Gln82Arg
ENST00000651583.1:c.200A>G	ENSP00000498821.1:p.Gln67Arg
ENST00000219066.5:c.269A>G	ENSP00000219066.1:p.Gln90Arg
ENST00000561841.1:c.165A>G
ENST00000566380.5:c.208A>G
ENST00000568513.5:c.173+43A>G
NM_002528.5:c.269A>G	NP_002519.1:p.Gln90Arg
XM_011522505.1:c.269A>G	XP_011520807.1:p.Gln90Arg
NM_001318193.1:c.269A>G	NP_001305122.1:p.Gln90Arg
NM_001318194.1:c.24+43A>G	NP_001305123.1:n.24+43A>G
NM_002528.6:c.269A>G	NP_002519.1:p.Gln90Arg
XM_017023253.1:c.269A>G	XP_016878742.1:p.Gln90Arg
NM_001318193.2:c.245A>G	NP_001305122.2:p.Gln82Arg
NM_002528.7:c.245A>G MANE Select	NP_002519.2:p.Gln82Arg
NM_001318194.2:c.24+43A>G	NP_001305123.1:n.24+43A>G