Canonical Allele Identifier: CA1619384328

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969384G= , CM000668.2:g.31969384G=	GRCh38
NC_000006.11:g.31937161G= , CM000668.1:g.31937161G=	GRCh37
NC_000006.10:g.32045140G=	NCBI36
NG_032652.1:g.15581G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2458G=	ENSP00000419905.1:n.*2458G=
ENST00000483553.6:c.*471G=	ENSP00000420332.2:n.*471G=
ENST00000485349.6:n.3980G=
ENST00000491994.2:c.3504G=	ENSP00000417586.2:p.Gly1168=
ENST00000494058.6:n.3806G=
ENST00000697831.1:c.3435G=	ENSP00000513453.1:p.Gly1145=
ENST00000697832.1:n.3657G=
ENST00000697833.1:c.*452G=	ENSP00000513454.1:n.*452G=
ENST00000697834.1:n.4128G=
ENST00000697835.1:c.*3022G=	ENSP00000513455.1:n.*3022G=
ENST00000697836.1:n.3835G=
ENST00000697837.1:c.*620G=	ENSP00000513456.1:n.*620G=
ENST00000697838.1:c.3369G=	ENSP00000513457.1:p.Gly1123=
ENST00000697839.1:n.4222G=
ENST00000697840.1:c.3540G=	ENSP00000513458.1:p.Gly1180=
ENST00000697841.1:n.4321G=
ENST00000697842.1:n.3759G=
ENST00000375394.7:c.3504G= MANE Select	ENSP00000364543.2:p.Gly1168=
ENST00000375394.6:c.3504G=	ENSP00000364543.2:p.Gly1168=
ENST00000465703.5:n.4140G=
ENST00000470453.1:n.382+68G=
ENST00000471818.1:n.433G=
ENST00000474839.5:c.*2876G=	ENSP00000420470.1:n.*2876G=
ENST00000483553.5:c.940G=
ENST00000485349.5:n.710G=
ENST00000491994.1:c.499G=
NM_006929.4:c.3504G=	NP_008860.4:p.Gly1168=
XR_001743586.2:n.3603G=
XR_926301.3:n.3520G=
NM_006929.5:c.3504G= MANE Select	NP_008860.4:p.Gly1168=