Canonical Allele Identifier: CA2643259973

Gene: DISP3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11515861T>C , CM000663.2:g.11515861T>C	GRCh38
NC_000001.10:g.11575918T>C , CM000663.1:g.11575918T>C	GRCh37
NC_000001.9:g.11498505T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020780.2:c.1589-140T>C MANE Select	NP_065831.1:n.1589-140T>C
ENST00000294484.7:c.1589-140T>C MANE Select	ENSP00000294484.6:n.1589-140T>C
NM_020780.1:c.1589-140T>C	NP_065831.1:n.1589-140T>C
ENST00000294484.6:c.1589-140T>C	ENSP00000294484.6:n.1589-140T>C
XM_011541828.1:c.1589-140T>C	XP_011540130.1:n.1589-140T>C
XM_011541828.3:c.1589-140T>C	XP_011540130.1:n.1589-140T>C
XM_011541829.1:c.476-140T>C	XP_011540131.1:n.476-140T>C
XM_011541830.1:c.1589-140T>C	XP_011540132.1:n.1589-140T>C
XM_011541830.2:c.1589-140T>C	XP_011540132.1:n.1589-140T>C
XM_011541831.1:c.1589-140T>C	XP_011540133.1:n.1589-140T>C
XM_011541831.2:c.1589-140T>C	XP_011540133.1:n.1589-140T>C
XM_011541832.1:c.1589-140T>C	XP_011540134.1:n.1589-140T>C
XM_011541832.2:c.1589-140T>C	XP_011540134.1:n.1589-140T>C
XM_011541833.1:c.1589-140T>C	XP_011540135.1:n.1589-140T>C
XM_011541833.2:c.1589-140T>C	XP_011540135.1:n.1589-140T>C
XM_011541834.1:c.1589-140T>C	XP_011540136.1:n.1589-140T>C
XM_011541835.1:c.1589-140T>C	XP_011540137.1:n.1589-140T>C
XM_011541835.2:c.1589-140T>C	XP_011540137.1:n.1589-140T>C
XR_001737342.1:n.1810-140T>C
XR_946717.1:n.1614-140T>C
XR_946717.2:n.1810-140T>C