Canonical Allele Identifier: CA1110743697
Gene: NEIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11786406G>C , CM000670.2:g.11786406G>C GRCh38
NC_000008.10:g.11643915G>C , CM000670.1:g.11643915G>C GRCh37
NC_000008.9:g.11681324G>C NCBI36
NG_053043.1:g.21744G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000284503.7:c.*133G>C MANE Select ENSP00000284503.6:n.*133G>C
ENST00000284503.6:c.*133G>C ENSP00000284503.6:n.*133G>C
ENST00000403422.7:c.*133G>C ENSP00000384070.3:n.*133G>C
ENST00000436750.7:c.*133G>C ENSP00000394023.2:n.*133G>C
ENST00000455213.6:c.*133G>C ENSP00000397538.2:n.*133G>C
ENST00000524741.1:n.1232G>C
NM_001135746.1:c.*133G>C NP_001129218.1:n.*133G>C
NM_001135747.1:c.*133G>C NP_001129219.1:n.*133G>C
NM_001135748.1:c.*133G>C NP_001129220.1:n.*133G>C
NM_145043.2:c.*133G>C NP_659480.1:n.*133G>C
XM_005272381.1:c.*133G>C XP_005272438.1:n.*133G>C
XM_005272382.1:c.*133G>C XP_005272439.1:n.*133G>C
XM_005272383.1:c.*133G>C XP_005272440.1:n.*133G>C
NM_001135746.2:c.*133G>C NP_001129218.1:n.*133G>C
NM_001135747.2:c.*133G>C NP_001129219.1:n.*133G>C
NM_001135748.2:c.*133G>C NP_001129220.1:n.*133G>C
NM_001349439.1:c.*133G>C NP_001336368.1:n.*133G>C
NM_001349440.1:c.*133G>C NP_001336369.1:n.*133G>C
NM_001349441.1:c.*133G>C NP_001336370.1:n.*133G>C
NM_001349442.1:c.*133G>C NP_001336371.1:n.*133G>C
NM_145043.3:c.*133G>C NP_659480.1:n.*133G>C
NR_146180.1:n.1873G>C
NR_146181.1:n.2040G>C
NR_146182.1:n.948G>C
NM_145043.4:c.*133G>C MANE Select NP_659480.1:n.*133G>C
NM_001135746.3:c.*133G>C NP_001129218.1:n.*133G>C
NM_001135747.3:c.*133G>C NP_001129219.1:n.*133G>C
NM_001135748.3:c.*133G>C NP_001129220.1:n.*133G>C
NM_001349439.2:c.*133G>C NP_001336368.1:n.*133G>C
NM_001349440.2:c.*133G>C NP_001336369.1:n.*133G>C
NM_001349441.2:c.*133G>C NP_001336370.1:n.*133G>C
NM_001349442.2:c.*133G>C NP_001336371.1:n.*133G>C
NR_146180.2:n.1788G>C
NR_146181.2:n.1955G>C
NR_146182.2:n.863G>C