Canonical Allele Identifier: CA1619384351

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969430T= , CM000668.2:g.31969430T=	GRCh38
NC_000006.11:g.31937207T= , CM000668.1:g.31937207T=	GRCh37
NC_000006.10:g.32045186T=	NCBI36
NG_032652.1:g.15627T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2504T=	ENSP00000419905.1:n.*2504T=
ENST00000483553.6:c.*517T=	ENSP00000420332.2:n.*517T=
ENST00000485349.6:n.4016+10T=
ENST00000491994.2:c.3550T=	ENSP00000417586.2:p.Ter1184=
ENST00000494058.6:n.3842+10T=
ENST00000697831.1:c.3471+10T=	ENSP00000513453.1:n.3471+10T=
ENST00000697832.1:n.3693+10T=
ENST00000697833.1:c.*488+10T=	ENSP00000513454.1:n.*488+10T=
ENST00000697834.1:n.4174T=
ENST00000697835.1:c.*3058+10T=	ENSP00000513455.1:n.*3058+10T=
ENST00000697836.1:n.3871+10T=
ENST00000697837.1:c.*656+10T=	ENSP00000513456.1:n.*656+10T=
ENST00000697838.1:c.3405+10T=	ENSP00000513457.1:n.3405+10T=
ENST00000697839.1:n.4268T=
ENST00000697840.1:c.3576+10T=	ENSP00000513458.1:n.3576+10T=
ENST00000697841.1:n.4367T=
ENST00000697842.1:n.3795+10T=
ENST00000375394.7:c.3540+10T= MANE Select	ENSP00000364543.2:n.3540+10T=
ENST00000375394.6:c.3540+10T=	ENSP00000364543.2:n.3540+10T=
ENST00000465703.5:n.4186T=
ENST00000470453.1:n.383-85T=
ENST00000471818.1:n.469+10T=
ENST00000474839.5:c.*2912+10T=	ENSP00000420470.1:n.*2912+10T=
ENST00000483553.5:c.986T=
ENST00000491994.1:c.545T=
NM_006929.4:c.3540+10T=	NP_008860.4:n.3540+10T=
XR_001743586.2:n.3649T=
XR_926301.3:n.3556+10T=
NM_006929.5:c.3540+10T= MANE Select	NP_008860.4:n.3540+10T=