Canonical Allele Identifier: CA1776061983

Gene: UNC5D

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.35285438A= , CM000670.2:g.35285438A=	GRCh38
NC_000008.10:g.35142956A= , CM000670.1:g.35142956A=	GRCh37
NC_000008.9:g.35262498A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404895.7:c.103+49551A= MANE Select	ENSP00000385143.2:n.103+49551A=
ENST00000287272.6:c.103+49551A=	ENSP00000287272.2:n.103+49551A=
ENST00000404895.6:c.103+49551A=	ENSP00000385143.2:n.103+49551A=
ENST00000416672.5:c.103+49551A=	ENSP00000412652.1:n.103+49551A=
ENST00000420357.5:c.103+49551A=	ENSP00000392739.1:n.103+49551A=
NM_080872.2:c.103+49551A=	NP_543148.2:n.103+49551A=
XM_006716288.2:c.103+49551A=	XP_006716351.2:n.103+49551A=
XM_011544398.1:c.103+49551A=	XP_011542700.1:n.103+49551A=
XM_011544399.1:c.103+49551A=	XP_011542701.1:n.103+49551A=
XM_011544400.1:c.103+49551A=	XP_011542702.1:n.103+49551A=
XM_011544401.1:c.103+49551A=	XP_011542703.1:n.103+49551A=
XM_011544402.1:c.103+49551A=	XP_011542704.1:n.103+49551A=
XM_011544403.1:c.103+49551A=	XP_011542705.1:n.103+49551A=
XM_011544404.1:c.103+49551A=	XP_011542706.1:n.103+49551A=
NM_080872.3:c.103+49551A=	NP_543148.2:n.103+49551A=
XM_011544400.2:c.103+49551A=	XP_011542702.1:n.103+49551A=
XM_011544401.3:c.103+49551A=	XP_011542703.1:n.103+49551A=
XM_011544402.2:c.103+49551A=	XP_011542704.1:n.103+49551A=
XM_011544403.2:c.103+49551A=	XP_011542705.1:n.103+49551A=
XM_011544404.2:c.103+49551A=	XP_011542706.1:n.103+49551A=
XM_017013044.1:c.103+49551A=	XP_016868533.1:n.103+49551A=
XM_017013045.1:c.103+49551A=	XP_016868534.1:n.103+49551A=
XM_017013046.1:c.103+49551A=	XP_016868535.1:n.103+49551A=
XM_017013047.1:c.103+49551A=	XP_016868536.1:n.103+49551A=
XM_017013048.1:c.-138+25241A=	XP_016868537.1:n.-138+25241A=
XM_017013049.1:c.-138+25290A=	XP_016868538.1:n.-138+25290A=
XM_017013050.1:c.-138+25241A=	XP_016868539.1:n.-138+25241A=
NM_080872.4:c.103+49551A= MANE Select	NP_543148.2:n.103+49551A=