Canonical Allele Identifier: CA1619384403

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969579G= , CM000668.2:g.31969579G=	GRCh38
NC_000006.11:g.31937356G= , CM000668.1:g.31937356G=	GRCh37
NC_000006.10:g.32045335G=	NCBI36
NG_032652.1:g.15776G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2653G=	ENSP00000419905.1:n.*2653G=
ENST00000485349.6:n.4081G=
ENST00000491994.2:c.*147G=	ENSP00000417586.2:n.*147G=
ENST00000494058.6:n.3907G=
ENST00000697831.1:c.3536G=	ENSP00000513453.1:p.Arg1179=
ENST00000697832.1:n.3758G=
ENST00000697833.1:c.*553G=	ENSP00000513454.1:n.*553G=
ENST00000697834.1:n.4323G=
ENST00000697835.1:c.*3123G=	ENSP00000513455.1:n.*3123G=
ENST00000697836.1:n.3959G=
ENST00000697837.1:c.*721G=	ENSP00000513456.1:n.*721G=
ENST00000697838.1:c.3470G=	ENSP00000513457.1:p.Arg1157=
ENST00000697839.1:n.4417G=
ENST00000697840.1:c.3641G=	ENSP00000513458.1:p.Arg1214=
ENST00000697841.1:n.4516G=
ENST00000697842.1:n.3860G=
ENST00000375394.7:c.3605G= MANE Select	ENSP00000364543.2:p.Arg1202=
ENST00000375394.6:c.3605G=	ENSP00000364543.2:p.Arg1202=
ENST00000465703.5:n.4335G=
ENST00000470453.1:n.447G=
ENST00000471818.1:n.534G=
ENST00000474839.5:c.*2977G=	ENSP00000420470.1:n.*2977G=
ENST00000483553.5:c.1135G=
ENST00000491994.1:c.694G=
NM_006929.4:c.3605G=	NP_008860.4:p.Arg1202=
XR_926301.3:n.3621G=
NM_006929.5:c.3605G= MANE Select	NP_008860.4:p.Arg1202=