Canonical Allele Identifier: CA1565024414

Gene: SKIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516711A= , CM000667.2:g.95516711A=	GRCh38
NC_000005.9:g.94852415A= , CM000667.1:g.94852415A=	GRCh37
NC_000005.8:g.94878171A=	NCBI36
NG_023414.1:g.43295T= , LRG_173:g.43295T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506007.2:n.2931T=
ENST00000513232.2:c.*1356T=	ENSP00000422749.2:n.*1356T=
ENST00000698450.1:n.1860T=
ENST00000698451.1:n.2061T=
ENST00000698452.1:n.3132T=
ENST00000698453.1:c.2442-125T=	ENSP00000513735.1:n.2442-125T=
ENST00000698454.1:c.2467T=	ENSP00000513736.1:p.Leu823=
ENST00000698455.1:c.*2617T=	ENSP00000513737.1:n.*2617T=
ENST00000698456.1:c.*1334T=	ENSP00000513738.1:n.*1334T=
ENST00000698457.1:c.2266T=	ENSP00000513739.1:p.Leu756=
ENST00000698458.1:c.2478-125T=	ENSP00000513740.1:n.2478-125T=
ENST00000698459.1:c.2476T=	ENSP00000513741.1:p.Leu826=
ENST00000698460.1:c.*279-125T=	ENSP00000513742.1:n.*279-125T=
ENST00000698461.1:n.2931T=
ENST00000698462.1:n.2851T=
ENST00000698468.1:n.3132T=
ENST00000698469.1:c.*1988T=	ENSP00000513743.1:n.*1988T=
ENST00000698470.1:c.*483T=	ENSP00000513744.1:n.*483T=
ENST00000698471.1:n.2931T=
ENST00000698472.1:c.*1356T=	ENSP00000513745.1:n.*1356T=
ENST00000698473.1:n.2931T=
ENST00000698474.1:n.2931T=
ENST00000698475.1:n.3016T=
ENST00000698476.1:c.2476T=	ENSP00000513746.1:p.Leu826=
ENST00000698477.1:c.2442-125T=	ENSP00000513747.1:n.2442-125T=
ENST00000698478.1:n.2931T=
ENST00000698479.1:c.2476T=	ENSP00000513748.1:p.Leu826=
ENST00000698480.1:c.2437-125T=	ENSP00000513749.1:n.2437-125T=
ENST00000698481.1:c.2437-125T=	ENSP00000513750.1:n.2437-125T=
ENST00000698482.1:n.2766T=
ENST00000698483.1:n.2931T=
ENST00000698484.1:c.2476T=	ENSP00000513751.1:p.Leu826=
ENST00000698485.1:c.2437-125T=	ENSP00000513752.1:n.2437-125T=
ENST00000698486.1:n.2931T=
ENST00000698487.1:c.2476T=	ENSP00000513753.1:p.Leu826=
ENST00000698488.1:c.2260-125T=	ENSP00000513754.1:n.2260-125T=
ENST00000698489.1:n.6716T=
ENST00000698490.1:c.2476T=	ENSP00000513755.1:p.Leu826=
ENST00000698492.1:c.*1191T=	ENSP00000513756.1:n.*1191T=
ENST00000698493.1:n.2766T=
ENST00000698494.1:c.*371T=	ENSP00000513757.1:n.*371T=
ENST00000358746.7:c.2476T= MANE Select	ENSP00000351596.3:p.Leu826=
ENST00000649566.1:c.2476T=	ENSP00000497948.1:p.Leu826=
ENST00000358746.6:c.2476T=	ENSP00000351596.2:p.Leu826=
ENST00000506007.1:n.58T=
ENST00000507805.5:n.663T=
NM_014639.3:c.2476T= , LRG_173t1:c.2476T=	NP_055454.1:p.Leu826=
XR_948312.1:n.2745T=
XR_001742370.2:n.2748T=
NM_014639.4:c.2476T= MANE Select	NP_055454.1:p.Leu826=