Canonical Allele Identifier: CA492953314

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096240G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046239G>T , CM000678.2:g.2046239G>T	GRCh38
NC_000016.9:g.2096240G>T , CM000678.1:g.2096240G>T	GRCh37
NC_000016.8:g.2036241G>T	NCBI36
NG_005895.1:g.1934G>T , LRG_487:g.1934G>T
NG_008412.1:g.6628C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.243C>A MANE Select	ENSP00000498421.1:p.Pro81=
ENST00000651583.1:c.198C>A	ENSP00000498821.1:p.Pro66=
ENST00000219066.5:c.267C>A	ENSP00000219066.1:p.Pro89=
ENST00000561841.1:c.163C>A
ENST00000566380.5:c.206C>A
ENST00000568513.5:c.173+41C>A
NM_002528.5:c.267C>A	NP_002519.1:p.Pro89=
XM_011522505.1:c.267C>A	XP_011520807.1:p.Pro89=
NM_001318193.1:c.267C>A	NP_001305122.1:p.Pro89=
NM_001318194.1:c.24+41C>A	NP_001305123.1:n.24+41C>A
NM_002528.6:c.267C>A	NP_002519.1:p.Pro89=
XM_017023253.1:c.267C>A	XP_016878742.1:p.Pro89=
NM_001318193.2:c.243C>A	NP_001305122.2:p.Pro81=
NM_002528.7:c.243C>A MANE Select	NP_002519.2:p.Pro81=
NM_001318194.2:c.24+41C>A	NP_001305123.1:n.24+41C>A