Canonical Allele Identifier: CA445717339

Gene: SKIC3

Linked Data

• MyVariant Identifiers: chr5:g.94852436T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516732T>G , CM000667.2:g.95516732T>G	GRCh38
NC_000005.9:g.94852436T>G , CM000667.1:g.94852436T>G	GRCh37
NC_000005.8:g.94878192T>G	NCBI36
NG_023414.1:g.43274A>C , LRG_173:g.43274A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506007.2:n.2910A>C
ENST00000513232.2:c.*1335A>C	ENSP00000422749.2:n.*1335A>C
ENST00000698450.1:n.1839A>C
ENST00000698451.1:n.2040A>C
ENST00000698452.1:n.3111A>C
ENST00000698453.1:c.2442-146A>C	ENSP00000513735.1:n.2442-146A>C
ENST00000698454.1:c.2446A>C	ENSP00000513736.1:p.Arg816=
ENST00000698455.1:c.*2596A>C	ENSP00000513737.1:n.*2596A>C
ENST00000698456.1:c.*1313A>C	ENSP00000513738.1:n.*1313A>C
ENST00000698457.1:c.2245A>C	ENSP00000513739.1:p.Arg749=
ENST00000698458.1:c.2478-146A>C	ENSP00000513740.1:n.2478-146A>C
ENST00000698459.1:c.2455A>C	ENSP00000513741.1:p.Arg819=
ENST00000698460.1:c.*279-146A>C	ENSP00000513742.1:n.*279-146A>C
ENST00000698461.1:n.2910A>C
ENST00000698462.1:n.2830A>C
ENST00000698468.1:n.3111A>C
ENST00000698469.1:c.*1967A>C	ENSP00000513743.1:n.*1967A>C
ENST00000698470.1:c.*462A>C	ENSP00000513744.1:n.*462A>C
ENST00000698471.1:n.2910A>C
ENST00000698472.1:c.*1335A>C	ENSP00000513745.1:n.*1335A>C
ENST00000698473.1:n.2910A>C
ENST00000698474.1:n.2910A>C
ENST00000698475.1:n.2995A>C
ENST00000698476.1:c.2455A>C	ENSP00000513746.1:p.Arg819=
ENST00000698477.1:c.2442-146A>C	ENSP00000513747.1:n.2442-146A>C
ENST00000698478.1:n.2910A>C
ENST00000698479.1:c.2455A>C	ENSP00000513748.1:p.Arg819=
ENST00000698480.1:c.2437-146A>C	ENSP00000513749.1:n.2437-146A>C
ENST00000698481.1:c.2437-146A>C	ENSP00000513750.1:n.2437-146A>C
ENST00000698482.1:n.2745A>C
ENST00000698483.1:n.2910A>C
ENST00000698484.1:c.2455A>C	ENSP00000513751.1:p.Arg819=
ENST00000698485.1:c.2437-146A>C	ENSP00000513752.1:n.2437-146A>C
ENST00000698486.1:n.2910A>C
ENST00000698487.1:c.2455A>C	ENSP00000513753.1:p.Arg819=
ENST00000698488.1:c.2260-146A>C	ENSP00000513754.1:n.2260-146A>C
ENST00000698489.1:n.6695A>C
ENST00000698490.1:c.2455A>C	ENSP00000513755.1:p.Arg819=
ENST00000698492.1:c.*1170A>C	ENSP00000513756.1:n.*1170A>C
ENST00000698493.1:n.2745A>C
ENST00000698494.1:c.*350A>C	ENSP00000513757.1:n.*350A>C
ENST00000358746.7:c.2455A>C MANE Select	ENSP00000351596.3:p.Arg819=
ENST00000649566.1:c.2455A>C	ENSP00000497948.1:p.Arg819=
ENST00000358746.6:c.2455A>C	ENSP00000351596.2:p.Arg819=
ENST00000506007.1:n.37A>C
ENST00000507805.5:n.642A>C
NM_014639.3:c.2455A>C , LRG_173t1:c.2455A>C	NP_055454.1:p.Arg819=
XR_948312.1:n.2724A>C
XR_001742370.2:n.2727A>C
NM_014639.4:c.2455A>C MANE Select	NP_055454.1:p.Arg819=