Canonical Allele Identifier: CA1619384342

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969413G= , CM000668.2:g.31969413G=	GRCh38
NC_000006.11:g.31937190G= , CM000668.1:g.31937190G=	GRCh37
NC_000006.10:g.32045169G=	NCBI36
NG_032652.1:g.15610G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2487G=	ENSP00000419905.1:n.*2487G=
ENST00000483553.6:c.*500G=	ENSP00000420332.2:n.*500G=
ENST00000485349.6:n.4009G=
ENST00000491994.2:c.3533G=	ENSP00000417586.2:p.Arg1178=
ENST00000494058.6:n.3835G=
ENST00000697831.1:c.3464G=	ENSP00000513453.1:p.Arg1155=
ENST00000697832.1:n.3686G=
ENST00000697833.1:c.*481G=	ENSP00000513454.1:n.*481G=
ENST00000697834.1:n.4157G=
ENST00000697835.1:c.*3051G=	ENSP00000513455.1:n.*3051G=
ENST00000697836.1:n.3864G=
ENST00000697837.1:c.*649G=	ENSP00000513456.1:n.*649G=
ENST00000697838.1:c.3398G=	ENSP00000513457.1:p.Arg1133=
ENST00000697839.1:n.4251G=
ENST00000697840.1:c.3569G=	ENSP00000513458.1:p.Arg1190=
ENST00000697841.1:n.4350G=
ENST00000697842.1:n.3788G=
ENST00000375394.7:c.3533G= MANE Select	ENSP00000364543.2:p.Arg1178=
ENST00000375394.6:c.3533G=	ENSP00000364543.2:p.Arg1178=
ENST00000465703.5:n.4169G=
ENST00000470453.1:n.382+97G=
ENST00000471818.1:n.462G=
ENST00000474839.5:c.*2905G=	ENSP00000420470.1:n.*2905G=
ENST00000483553.5:c.969G=
ENST00000491994.1:c.528G=
NM_006929.4:c.3533G=	NP_008860.4:p.Arg1178=
XR_001743586.2:n.3632G=
XR_926301.3:n.3549G=
NM_006929.5:c.3533G= MANE Select	NP_008860.4:p.Arg1178=