Canonical Allele Identifier: CA1619384358

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969454C= , CM000668.2:g.31969454C=	GRCh38
NC_000006.11:g.31937231C= , CM000668.1:g.31937231C=	GRCh37
NC_000006.10:g.32045210C=	NCBI36
NG_032652.1:g.15651C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2528C=	ENSP00000419905.1:n.*2528C=
ENST00000483553.6:c.*541C=	ENSP00000420332.2:n.*541C=
ENST00000485349.6:n.4016+34C=
ENST00000491994.2:c.*22C=	ENSP00000417586.2:n.*22C=
ENST00000494058.6:n.3842+34C=
ENST00000697831.1:c.3471+34C=	ENSP00000513453.1:n.3471+34C=
ENST00000697832.1:n.3693+34C=
ENST00000697833.1:c.*488+34C=	ENSP00000513454.1:n.*488+34C=
ENST00000697834.1:n.4198C=
ENST00000697835.1:c.*3058+34C=	ENSP00000513455.1:n.*3058+34C=
ENST00000697836.1:n.3871+34C=
ENST00000697837.1:c.*656+34C=	ENSP00000513456.1:n.*656+34C=
ENST00000697838.1:c.3405+34C=	ENSP00000513457.1:n.3405+34C=
ENST00000697839.1:n.4292C=
ENST00000697840.1:c.3576+34C=	ENSP00000513458.1:n.3576+34C=
ENST00000697841.1:n.4391C=
ENST00000697842.1:n.3795+34C=
ENST00000375394.7:c.3540+34C= MANE Select	ENSP00000364543.2:n.3540+34C=
ENST00000375394.6:c.3540+34C=	ENSP00000364543.2:n.3540+34C=
ENST00000465703.5:n.4210C=
ENST00000470453.1:n.383-61C=
ENST00000471818.1:n.469+34C=
ENST00000474839.5:c.*2912+34C=	ENSP00000420470.1:n.*2912+34C=
ENST00000483553.5:c.1010C=
ENST00000491994.1:c.569C=
NM_006929.4:c.3540+34C=	NP_008860.4:n.3540+34C=
XR_001743586.2:n.3673C=
XR_926301.3:n.3556+34C=
NM_006929.5:c.3540+34C= MANE Select	NP_008860.4:n.3540+34C=