Canonical Allele Identifier: CA2202016908

Gene: NTHL1

Linked Data

• dbSNP Id: rs2084355781
• gnomAD v4: 16-2046050-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046054del , CM000678.2:g.2046054del	GRCh38
NC_000016.9:g.2096055del , CM000678.1:g.2096055del	GRCh37
NC_000016.8:g.2036056del	NCBI36
NG_005895.1:g.1749del , LRG_487:g.1749del
NG_008412.1:g.6816del

Transcript Alleles

HGVS	Amino-acid change
ENST00000651522.1:c.63+77del	ENSP00000498290.1:n.63+77del
ENST00000651570.2:c.354+77del MANE Select	ENSP00000498421.1:n.354+77del
ENST00000651583.1:c.309+77del	ENSP00000498821.1:n.309+77del
ENST00000219066.5:c.378+77del	ENSP00000219066.1:n.378+77del
ENST00000561841.1:c.274+77del
ENST00000562120.1:n.87+77del
ENST00000566380.5:c.317+77del
ENST00000568513.5:c.173+229del
NM_002528.5:c.378+77del	NP_002519.1:n.378+77del
XM_011522505.1:c.378+77del	XP_011520807.1:n.378+77del
NM_001318193.1:c.378+77del	NP_001305122.1:n.378+77del
NM_001318194.1:c.24+229del	NP_001305123.1:n.24+229del
NM_002528.6:c.378+77del	NP_002519.1:n.378+77del
XM_017023253.1:c.378+77del	XP_016878742.1:n.378+77del
NM_001318193.2:c.354+77del	NP_001305122.2:n.354+77del
NM_002528.7:c.354+77del MANE Select	NP_002519.2:n.354+77del
NM_001318194.2:c.24+229del	NP_001305123.1:n.24+229del