Canonical Allele Identifier: CA492953300

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096219C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046218C>G , CM000678.2:g.2046218C>G	GRCh38
NC_000016.9:g.2096219C>G , CM000678.1:g.2096219C>G	GRCh37
NC_000016.8:g.2036220C>G	NCBI36
NG_005895.1:g.1913C>G , LRG_487:g.1913C>G
NG_008412.1:g.6649G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.264G>C MANE Select	ENSP00000498421.1:p.Leu88=
ENST00000651583.1:c.219G>C	ENSP00000498821.1:p.Leu73=
ENST00000219066.5:c.288G>C	ENSP00000219066.1:p.Leu96=
ENST00000561841.1:c.184G>C
ENST00000566380.5:c.227G>C
ENST00000568513.5:c.173+62G>C
NM_002528.5:c.288G>C	NP_002519.1:p.Leu96=
XM_011522505.1:c.288G>C	XP_011520807.1:p.Leu96=
NM_001318193.1:c.288G>C	NP_001305122.1:p.Leu96=
NM_001318194.1:c.24+62G>C	NP_001305123.1:n.24+62G>C
NM_002528.6:c.288G>C	NP_002519.1:p.Leu96=
XM_017023253.1:c.288G>C	XP_016878742.1:p.Leu96=
NM_001318193.2:c.264G>C	NP_001305122.2:p.Leu88=
NM_002528.7:c.264G>C MANE Select	NP_002519.2:p.Leu88=
NM_001318194.2:c.24+62G>C	NP_001305123.1:n.24+62G>C