Canonical Allele Identifier: CA1619377413

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960357G= , CM000668.2:g.31960357G=	GRCh38
NC_000006.11:g.31928134G= , CM000668.1:g.31928134G=	GRCh37
NC_000006.10:g.32036113G=	NCBI36
NG_032652.1:g.6554G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.354+20G=	ENSP00000419905.1:n.354+20G=
ENST00000483553.6:c.354+20G=	ENSP00000420332.2:n.354+20G=
ENST00000485349.6:n.395+20G=
ENST00000491994.2:c.354+20G=	ENSP00000417586.2:n.354+20G=
ENST00000494058.6:n.411+20G=
ENST00000697831.1:c.354+20G=	ENSP00000513453.1:n.354+20G=
ENST00000697832.1:n.430+20G=
ENST00000697833.1:c.354+20G=	ENSP00000513454.1:n.354+20G=
ENST00000697834.1:n.406+20G=
ENST00000697835.1:c.373+20G=	ENSP00000513455.1:n.373+20G=
ENST00000697836.1:n.390+20G=
ENST00000697837.1:c.354+20G=	ENSP00000513456.1:n.354+20G=
ENST00000697838.1:c.219+20G=	ENSP00000513457.1:n.219+20G=
ENST00000697839.1:n.376+20G=
ENST00000697840.1:c.354+20G=	ENSP00000513458.1:n.354+20G=
ENST00000697841.1:n.365+20G=
ENST00000697842.1:n.354+20G=
ENST00000375394.7:c.354+20G= MANE Select	ENSP00000364543.2:n.354+20G=
ENST00000375394.6:c.354+20G=	ENSP00000364543.2:n.354+20G=
ENST00000461073.5:c.354+20G=	ENSP00000419905.1:n.354+20G=
ENST00000465703.5:n.406+20G=
ENST00000474839.5:c.127-684G=	ENSP00000420470.1:n.127-684G=
ENST00000488648.5:n.430+20G=
ENST00000628157.1:c.127-684G=	ENSP00000485707.1:n.127-684G=
NM_006929.4:c.354+20G=	NP_008860.4:n.354+20G=
XM_006715168.2:c.354+20G=	XP_006715231.1:n.354+20G=
XM_011514815.1:c.354+20G=	XP_011513117.1:n.354+20G=
XR_926301.1:n.442+20G=
XM_011514815.3:c.354+20G=	XP_011513117.1:n.354+20G=
XR_001743586.2:n.390+20G=
XR_926301.3:n.390+20G=
NM_006929.5:c.354+20G= MANE Select	NP_008860.4:n.354+20G=