Canonical Allele Identifier: CA1619384415

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969606G= , CM000668.2:g.31969606G=	GRCh38
NC_000006.11:g.31937383G= , CM000668.1:g.31937383G=	GRCh37
NC_000006.10:g.32045362G=	NCBI36
NG_032652.1:g.15803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2680G=	ENSP00000419905.1:n.*2680G=
ENST00000485349.6:n.4108G=
ENST00000491994.2:c.*174G=	ENSP00000417586.2:n.*174G=
ENST00000494058.6:n.3934G=
ENST00000697831.1:c.3563G=	ENSP00000513453.1:p.Arg1188=
ENST00000697832.1:n.3785G=
ENST00000697834.1:n.4350G=
ENST00000697835.1:c.*3150G=	ENSP00000513455.1:n.*3150G=
ENST00000697836.1:n.3986G=
ENST00000697837.1:c.*748G=	ENSP00000513456.1:n.*748G=
ENST00000697838.1:c.3497G=	ENSP00000513457.1:p.Arg1166=
ENST00000697839.1:n.4444G=
ENST00000697840.1:c.3668G=	ENSP00000513458.1:p.Arg1223=
ENST00000697841.1:n.4543G=
ENST00000697842.1:n.3887G=
ENST00000375394.7:c.3632G= MANE Select	ENSP00000364543.2:p.Arg1211=
ENST00000375394.6:c.3632G=	ENSP00000364543.2:p.Arg1211=
ENST00000465703.5:n.4362G=
ENST00000471818.1:n.561G=
ENST00000474839.5:c.*3004G=	ENSP00000420470.1:n.*3004G=
ENST00000483553.5:c.1162G=
ENST00000491994.1:c.721G=
NM_006929.4:c.3632G=	NP_008860.4:p.Arg1211=
XR_926301.3:n.3648G=
NM_006929.5:c.3632G= MANE Select	NP_008860.4:p.Arg1211=