Canonical Allele Identifier: CA1324702523

Gene: UNC80

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.209775903G= , CM000664.2:g.209775903G=	GRCh38
NC_000002.11:g.210640627G= , CM000664.1:g.210640627G=	GRCh37
NC_000002.10:g.210348872G=	NCBI36
NG_051361.1:g.8979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673920.1:c.156G= MANE Select	ENSP00000501211.1:p.Val52=
ENST00000673951.1:c.156G=	ENSP00000501012.1:p.Val52=
ENST00000272845.10:c.156G=	ENSP00000272845.5:p.Val52=
ENST00000439458.5:c.156G=	ENSP00000391088.1:p.Val52=
ENST00000478701.1:n.236G=
NM_032504.1:c.156G=	NP_115893.1:p.Val52=
NM_182587.3:c.156G=	NP_872393.3:p.Val52=
XM_005246476.1:c.156G=	XP_005246533.1:p.Val52=
XM_011511004.1:c.156G=	XP_011509306.1:p.Val52=
XM_011511005.1:c.156G=	XP_011509307.1:p.Val52=
XM_011511006.1:c.156G=	XP_011509308.1:p.Val52=
XM_011511007.1:c.156G=	XP_011509309.1:p.Val52=
XM_011511008.1:c.156G=	XP_011509310.1:p.Val52=
XM_011511009.1:c.156G=	XP_011509311.1:p.Val52=
XM_011511010.1:c.156G=	XP_011509312.1:p.Val52=
XM_011511011.1:c.156G=	XP_011509313.1:p.Val52=
XM_011511012.1:c.156G=	XP_011509314.1:p.Val52=
XM_011511010.2:c.156G=	XP_011509312.1:p.Val52=
XM_017003884.1:c.156G=	XP_016859373.1:p.Val52=
XM_017003885.1:c.156G=	XP_016859374.1:p.Val52=
XM_017003886.1:c.156G=	XP_016859375.1:p.Val52=
XM_017003887.1:c.156G=	XP_016859376.1:p.Val52=
XM_017003888.1:c.156G=	XP_016859377.1:p.Val52=
XM_017003889.1:c.156G=	XP_016859378.1:p.Val52=
XM_017003890.1:c.156G=	XP_016859379.1:p.Val52=
XM_017003891.1:c.-199G=	XP_016859380.1:n.-199G=
XM_017003893.1:c.156G=	XP_016859382.1:p.Val52=
XR_002959283.1:n.236G=
NM_001371986.1:c.156G= MANE Select	NP_001358915.1:p.Val52=
NM_182587.4:c.156G=	NP_872393.3:p.Val52=
NM_032504.2:c.156G=	NP_115893.1:p.Val52=