Canonical Allele Identifier: CA394295137

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096148T>A (hg19) ; chr16:g.2046147T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046147T>A , CM000678.2:g.2046147T>A	GRCh38
NC_000016.9:g.2096148T>A , CM000678.1:g.2096148T>A	GRCh37
NC_000016.8:g.2036149T>A	NCBI36
NG_005895.1:g.1842T>A , LRG_487:g.1842T>A
NG_008412.1:g.6720A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651522.1:c.44A>T	ENSP00000498290.1:p.Asp15Val
ENST00000651570.2:c.335A>T MANE Select	ENSP00000498421.1:p.Asp112Val
ENST00000651583.1:c.290A>T	ENSP00000498821.1:p.Asp97Val
ENST00000219066.5:c.359A>T	ENSP00000219066.1:p.Asp120Val
ENST00000561841.1:c.255A>T
ENST00000562120.1:n.68A>T
ENST00000566380.5:c.298A>T
ENST00000568513.5:c.173+133A>T
NM_002528.5:c.359A>T	NP_002519.1:p.Asp120Val
XM_011522505.1:c.359A>T	XP_011520807.1:p.Asp120Val
NM_001318193.1:c.359A>T	NP_001305122.1:p.Asp120Val
NM_001318194.1:c.24+133A>T	NP_001305123.1:n.24+133A>T
NM_002528.6:c.359A>T	NP_002519.1:p.Asp120Val
XM_017023253.1:c.359A>T	XP_016878742.1:p.Asp120Val
NM_001318193.2:c.335A>T	NP_001305122.2:p.Asp112Val
NM_002528.7:c.335A>T MANE Select	NP_002519.2:p.Asp112Val
NM_001318194.2:c.24+133A>T	NP_001305123.1:n.24+133A>T