Canonical Allele Identifier: CA394295187

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096152A>T (hg19) ; chr16:g.2046151A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046151A>T , CM000678.2:g.2046151A>T	GRCh38
NC_000016.9:g.2096152A>T , CM000678.1:g.2096152A>T	GRCh37
NC_000016.8:g.2036153A>T	NCBI36
NG_005895.1:g.1846A>T , LRG_487:g.1846A>T
NG_008412.1:g.6716T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000651522.1:c.40T>A	ENSP00000498290.1:p.Tyr14Asn
ENST00000651570.2:c.331T>A MANE Select	ENSP00000498421.1:p.Tyr111Asn
ENST00000651583.1:c.286T>A	ENSP00000498821.1:p.Tyr96Asn
ENST00000219066.5:c.355T>A	ENSP00000219066.1:p.Tyr119Asn
ENST00000561841.1:c.251T>A
ENST00000562120.1:n.64T>A
ENST00000566380.5:c.294T>A
ENST00000568513.5:c.173+129T>A
NM_002528.5:c.355T>A	NP_002519.1:p.Tyr119Asn
XM_011522505.1:c.355T>A	XP_011520807.1:p.Tyr119Asn
NM_001318193.1:c.355T>A	NP_001305122.1:p.Tyr119Asn
NM_001318194.1:c.24+129T>A	NP_001305123.1:n.24+129T>A
NM_002528.6:c.355T>A	NP_002519.1:p.Tyr119Asn
XM_017023253.1:c.355T>A	XP_016878742.1:p.Tyr119Asn
NM_001318193.2:c.331T>A	NP_001305122.2:p.Tyr111Asn
NM_002528.7:c.331T>A MANE Select	NP_002519.2:p.Tyr111Asn
NM_001318194.2:c.24+129T>A	NP_001305123.1:n.24+129T>A