Canonical Allele Identifier: CA358783892

Gene: NEIL3

Linked Data

• dbSNP Id: rs2048074
• MyVariant Identifiers: chr4:g.178274565A>T (hg19) ; chr4:g.177353411A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177353411A>T , CM000666.2:g.177353411A>T	GRCh38
NC_000004.11:g.178274565A>T , CM000666.1:g.178274565A>T	GRCh37
NC_000004.10:g.178511559A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264596.4:c.1143A>T MANE Select	ENSP00000264596.3:p.Arg381Ser
ENST00000264596.3:c.1143A>T	ENSP00000264596.3:p.Arg381Ser
ENST00000513321.1:c.*417A>T	ENSP00000424735.1:n.*417A>T
NM_018248.2:c.1143A>T	NP_060718.2:p.Arg381Ser
XR_939503.1:n.445+3584T>A
XR_939504.1:n.556+3584T>A
XR_939505.1:n.335+3584T>A
XR_939506.1:n.216+3584T>A
XM_017008360.1:c.1143A>T	XP_016863849.1:p.Arg381Ser
XR_001741926.1:n.360+3584T>A
NM_018248.3:c.1143A>T MANE Select	NP_060718.3:p.Arg381Ser