Canonical Allele Identifier: CA1619384325

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969372G= , CM000668.2:g.31969372G=	GRCh38
NC_000006.11:g.31937149G= , CM000668.1:g.31937149G=	GRCh37
NC_000006.10:g.32045128G=	NCBI36
NG_032652.1:g.15569G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2446G=	ENSP00000419905.1:n.*2446G=
ENST00000483553.6:c.*459G=	ENSP00000420332.2:n.*459G=
ENST00000485349.6:n.3968G=
ENST00000491994.2:c.3492G=	ENSP00000417586.2:p.Glu1164=
ENST00000494058.6:n.3794G=
ENST00000697831.1:c.3423G=	ENSP00000513453.1:p.Glu1141=
ENST00000697832.1:n.3645G=
ENST00000697833.1:c.*440G=	ENSP00000513454.1:n.*440G=
ENST00000697834.1:n.4116G=
ENST00000697835.1:c.*3010G=	ENSP00000513455.1:n.*3010G=
ENST00000697836.1:n.3823G=
ENST00000697837.1:c.*608G=	ENSP00000513456.1:n.*608G=
ENST00000697838.1:c.3357G=	ENSP00000513457.1:p.Glu1119=
ENST00000697839.1:n.4210G=
ENST00000697840.1:c.3528G=	ENSP00000513458.1:p.Glu1176=
ENST00000697841.1:n.4309G=
ENST00000697842.1:n.3747G=
ENST00000375394.7:c.3492G= MANE Select	ENSP00000364543.2:p.Glu1164=
ENST00000375394.6:c.3492G=	ENSP00000364543.2:p.Glu1164=
ENST00000465703.5:n.4128G=
ENST00000470453.1:n.382+56G=
ENST00000471818.1:n.421G=
ENST00000474839.5:c.*2864G=	ENSP00000420470.1:n.*2864G=
ENST00000483553.5:c.928G=
ENST00000485349.5:n.698G=
ENST00000491994.1:c.487G=
NM_006929.4:c.3492G=	NP_008860.4:p.Glu1164=
XR_001743586.2:n.3591G=
XR_926301.3:n.3508G=
NM_006929.5:c.3492G= MANE Select	NP_008860.4:p.Glu1164=