Canonical Allele Identifier: CA394295425

Gene: NTHL1

Linked Data

• dbSNP Id: rs747659604
• MyVariant Identifiers: chr16:g.2096175T>A (hg19) ; chr16:g.2046174T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046174T>A , CM000678.2:g.2046174T>A	GRCh38
NC_000016.9:g.2096175T>A , CM000678.1:g.2096175T>A	GRCh37
NC_000016.8:g.2036176T>A	NCBI36
NG_005895.1:g.1869T>A , LRG_487:g.1869T>A
NG_008412.1:g.6693A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.17A>T	ENSP00000498290.1:p.Asp6Val
ENST00000651570.2:c.308A>T MANE Select	ENSP00000498421.1:p.Asp103Val
ENST00000651583.1:c.263A>T	ENSP00000498821.1:p.Asp88Val
ENST00000219066.5:c.332A>T	ENSP00000219066.1:p.Asp111Val
ENST00000561841.1:c.228A>T
ENST00000562120.1:n.41A>T
ENST00000566380.5:c.271A>T
ENST00000568513.5:c.173+106A>T
NM_002528.5:c.332A>T	NP_002519.1:p.Asp111Val
XM_011522505.1:c.332A>T	XP_011520807.1:p.Asp111Val
NM_001318193.1:c.332A>T	NP_001305122.1:p.Asp111Val
NM_001318194.1:c.24+106A>T	NP_001305123.1:n.24+106A>T
NM_002528.6:c.332A>T	NP_002519.1:p.Asp111Val
XM_017023253.1:c.332A>T	XP_016878742.1:p.Asp111Val
NM_001318193.2:c.308A>T	NP_001305122.2:p.Asp103Val
NM_002528.7:c.308A>T MANE Select	NP_002519.2:p.Asp103Val
NM_001318194.2:c.24+106A>T	NP_001305123.1:n.24+106A>T