Canonical Allele Identifier: CA2201987020

Gene: NTHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046351T= , CM000678.2:g.2046351T=	GRCh38
NC_000016.9:g.2096352T= , CM000678.1:g.2096352T=	GRCh37
NC_000016.8:g.2036353T=	NCBI36
NG_005895.1:g.2046T= , LRG_487:g.2046T=
NG_008412.1:g.6516A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.131A= MANE Select	ENSP00000498421.1:p.His44=
ENST00000651583.1:c.86A=	ENSP00000498821.1:p.His29=
ENST00000219066.5:c.155A=	ENSP00000219066.1:p.His52=
ENST00000561841.1:c.51A=
ENST00000566380.5:c.94A=
ENST00000568513.5:c.102A=
NM_002528.5:c.155A=	NP_002519.1:p.His52=
XM_011522505.1:c.155A=	XP_011520807.1:p.His52=
NM_001318193.1:c.155A=	NP_001305122.1:p.His52=
NM_001318194.1:c.-48A=	NP_001305123.1:n.-48A=
NM_002528.6:c.155A=	NP_002519.1:p.His52=
XM_017023253.1:c.155A=	XP_016878742.1:p.His52=
NM_001318193.2:c.131A=	NP_001305122.2:p.His44=
NM_002528.7:c.131A= MANE Select	NP_002519.2:p.His44=
NM_001318194.2:c.-48A=	NP_001305123.1:n.-48A=