Canonical Allele Identifier: CA1565024408

Gene: SKIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516691A= , CM000667.2:g.95516691A=	GRCh38
NC_000005.9:g.94852395A= , CM000667.1:g.94852395A=	GRCh37
NC_000005.8:g.94878151A=	NCBI36
NG_023414.1:g.43315T= , LRG_173:g.43315T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506007.2:n.2951T=
ENST00000513232.2:c.*1376T=	ENSP00000422749.2:n.*1376T=
ENST00000698450.1:n.1880T=
ENST00000698451.1:n.2081T=
ENST00000698452.1:n.3152T=
ENST00000698453.1:c.2442-105T=	ENSP00000513735.1:n.2442-105T=
ENST00000698454.1:c.2487T=	ENSP00000513736.1:p.Gly829=
ENST00000698455.1:c.*2637T=	ENSP00000513737.1:n.*2637T=
ENST00000698456.1:c.*1354T=	ENSP00000513738.1:n.*1354T=
ENST00000698457.1:c.2286T=	ENSP00000513739.1:p.Gly762=
ENST00000698458.1:c.2478-105T=	ENSP00000513740.1:n.2478-105T=
ENST00000698459.1:c.2496T=	ENSP00000513741.1:p.Gly832=
ENST00000698460.1:c.*279-105T=	ENSP00000513742.1:n.*279-105T=
ENST00000698461.1:n.2951T=
ENST00000698462.1:n.2871T=
ENST00000698468.1:n.3152T=
ENST00000698469.1:c.*2008T=	ENSP00000513743.1:n.*2008T=
ENST00000698470.1:c.*503T=	ENSP00000513744.1:n.*503T=
ENST00000698471.1:n.2951T=
ENST00000698472.1:c.*1376T=	ENSP00000513745.1:n.*1376T=
ENST00000698473.1:n.2951T=
ENST00000698474.1:n.2951T=
ENST00000698475.1:n.3036T=
ENST00000698476.1:c.2496T=	ENSP00000513746.1:p.Gly832=
ENST00000698477.1:c.2442-105T=	ENSP00000513747.1:n.2442-105T=
ENST00000698478.1:n.2951T=
ENST00000698479.1:c.2496T=	ENSP00000513748.1:p.Gly832=
ENST00000698480.1:c.2437-105T=	ENSP00000513749.1:n.2437-105T=
ENST00000698481.1:c.2437-105T=	ENSP00000513750.1:n.2437-105T=
ENST00000698482.1:n.2786T=
ENST00000698483.1:n.2951T=
ENST00000698484.1:c.2496T=	ENSP00000513751.1:p.Gly832=
ENST00000698485.1:c.2437-105T=	ENSP00000513752.1:n.2437-105T=
ENST00000698486.1:n.2951T=
ENST00000698487.1:c.2496T=	ENSP00000513753.1:p.Gly832=
ENST00000698488.1:c.2260-105T=	ENSP00000513754.1:n.2260-105T=
ENST00000698489.1:n.6736T=
ENST00000698490.1:c.2496T=	ENSP00000513755.1:p.Gly832=
ENST00000698492.1:c.*1211T=	ENSP00000513756.1:n.*1211T=
ENST00000698493.1:n.2786T=
ENST00000698494.1:c.*391T=	ENSP00000513757.1:n.*391T=
ENST00000358746.7:c.2496T= MANE Select	ENSP00000351596.3:p.Gly832=
ENST00000649566.1:c.2496T=	ENSP00000497948.1:p.Gly832=
ENST00000358746.6:c.2496T=	ENSP00000351596.2:p.Gly832=
ENST00000506007.1:n.78T=
ENST00000507805.5:n.683T=
NM_014639.3:c.2496T= , LRG_173t1:c.2496T=	NP_055454.1:p.Gly832=
XR_948312.1:n.2765T=
XR_001742370.2:n.2768T=
NM_014639.4:c.2496T= MANE Select	NP_055454.1:p.Gly832=