Canonical Allele Identifier: CA492953236

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096177C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046176C>A , CM000678.2:g.2046176C>A	GRCh38
NC_000016.9:g.2096177C>A , CM000678.1:g.2096177C>A	GRCh37
NC_000016.8:g.2036178C>A	NCBI36
NG_005895.1:g.1871C>A , LRG_487:g.1871C>A
NG_008412.1:g.6691G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.15G>T	ENSP00000498290.1:p.Val5=
ENST00000651570.2:c.306G>T MANE Select	ENSP00000498421.1:p.Val102=
ENST00000651583.1:c.261G>T	ENSP00000498821.1:p.Val87=
ENST00000219066.5:c.330G>T	ENSP00000219066.1:p.Val110=
ENST00000561841.1:c.226G>T
ENST00000562120.1:n.39G>T
ENST00000566380.5:c.269G>T
ENST00000568513.5:c.173+104G>T
NM_002528.5:c.330G>T	NP_002519.1:p.Val110=
XM_011522505.1:c.330G>T	XP_011520807.1:p.Val110=
NM_001318193.1:c.330G>T	NP_001305122.1:p.Val110=
NM_001318194.1:c.24+104G>T	NP_001305123.1:n.24+104G>T
NM_002528.6:c.330G>T	NP_002519.1:p.Val110=
XM_017023253.1:c.330G>T	XP_016878742.1:p.Val110=
NM_001318193.2:c.306G>T	NP_001305122.2:p.Val102=
NM_002528.7:c.306G>T MANE Select	NP_002519.2:p.Val102=
NM_001318194.2:c.24+104G>T	NP_001305123.1:n.24+104G>T