Canonical Allele Identifier: CA1619384352

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969431G= , CM000668.2:g.31969431G=	GRCh38
NC_000006.11:g.31937208G= , CM000668.1:g.31937208G=	GRCh37
NC_000006.10:g.32045187G=	NCBI36
NG_032652.1:g.15628G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2505G=	ENSP00000419905.1:n.*2505G=
ENST00000483553.6:c.*518G=	ENSP00000420332.2:n.*518G=
ENST00000485349.6:n.4016+11G=
ENST00000491994.2:c.3551G=	ENSP00000417586.2:p.Ter1184=
ENST00000494058.6:n.3842+11G=
ENST00000697831.1:c.3471+11G=	ENSP00000513453.1:n.3471+11G=
ENST00000697832.1:n.3693+11G=
ENST00000697833.1:c.*488+11G=	ENSP00000513454.1:n.*488+11G=
ENST00000697834.1:n.4175G=
ENST00000697835.1:c.*3058+11G=	ENSP00000513455.1:n.*3058+11G=
ENST00000697836.1:n.3871+11G=
ENST00000697837.1:c.*656+11G=	ENSP00000513456.1:n.*656+11G=
ENST00000697838.1:c.3405+11G=	ENSP00000513457.1:n.3405+11G=
ENST00000697839.1:n.4269G=
ENST00000697840.1:c.3576+11G=	ENSP00000513458.1:n.3576+11G=
ENST00000697841.1:n.4368G=
ENST00000697842.1:n.3795+11G=
ENST00000375394.7:c.3540+11G= MANE Select	ENSP00000364543.2:n.3540+11G=
ENST00000375394.6:c.3540+11G=	ENSP00000364543.2:n.3540+11G=
ENST00000465703.5:n.4187G=
ENST00000470453.1:n.383-84G=
ENST00000471818.1:n.469+11G=
ENST00000474839.5:c.*2912+11G=	ENSP00000420470.1:n.*2912+11G=
ENST00000483553.5:c.987G=
ENST00000491994.1:c.546G=
NM_006929.4:c.3540+11G=	NP_008860.4:n.3540+11G=
XR_001743586.2:n.3650G=
XR_926301.3:n.3556+11G=
NM_006929.5:c.3540+11G= MANE Select	NP_008860.4:n.3540+11G=