Canonical Allele Identifier: CA2580799630

Gene: NEIL2

Genomic Alleles

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

Transcript Alleles

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