Canonical Allele Identifier: CA394297977

Gene: NTHL1

Linked Data

• MyVariant Identifiers: chr16:g.2096338G>T (hg19) ; chr16:g.2046337G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046337G>T , CM000678.2:g.2046337G>T	GRCh38
NC_000016.9:g.2096338G>T , CM000678.1:g.2096338G>T	GRCh37
NC_000016.8:g.2036339G>T	NCBI36
NG_005895.1:g.2032G>T , LRG_487:g.2032G>T
NG_008412.1:g.6530C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.145C>A MANE Select	ENSP00000498421.1:p.Arg49Ser
ENST00000651583.1:c.100C>A	ENSP00000498821.1:p.Arg34Ser
ENST00000219066.5:c.169C>A	ENSP00000219066.1:p.Arg57Ser
ENST00000561841.1:c.65C>A
ENST00000566380.5:c.108C>A
ENST00000568513.5:c.116C>A
NM_002528.5:c.169C>A	NP_002519.1:p.Arg57Ser
XM_011522505.1:c.169C>A	XP_011520807.1:p.Arg57Ser
NM_001318193.1:c.169C>A	NP_001305122.1:p.Arg57Ser
NM_001318194.1:c.-34C>A	NP_001305123.1:n.-34C>A
NM_002528.6:c.169C>A	NP_002519.1:p.Arg57Ser
XM_017023253.1:c.169C>A	XP_016878742.1:p.Arg57Ser
NM_001318193.2:c.145C>A	NP_001305122.2:p.Arg49Ser
NM_002528.7:c.145C>A MANE Select	NP_002519.2:p.Arg49Ser
NM_001318194.2:c.-34C>A	NP_001305123.1:n.-34C>A