Canonical Allele Identifier: CA1619384414

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969605C= , CM000668.2:g.31969605C=	GRCh38
NC_000006.11:g.31937382C= , CM000668.1:g.31937382C=	GRCh37
NC_000006.10:g.32045361C=	NCBI36
NG_032652.1:g.15802C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2679C=	ENSP00000419905.1:n.*2679C=
ENST00000485349.6:n.4107C=
ENST00000491994.2:c.*173C=	ENSP00000417586.2:n.*173C=
ENST00000494058.6:n.3933C=
ENST00000697831.1:c.3562C=	ENSP00000513453.1:p.Arg1188=
ENST00000697832.1:n.3784C=
ENST00000697834.1:n.4349C=
ENST00000697835.1:c.*3149C=	ENSP00000513455.1:n.*3149C=
ENST00000697836.1:n.3985C=
ENST00000697837.1:c.*747C=	ENSP00000513456.1:n.*747C=
ENST00000697838.1:c.3496C=	ENSP00000513457.1:p.Arg1166=
ENST00000697839.1:n.4443C=
ENST00000697840.1:c.3667C=	ENSP00000513458.1:p.Arg1223=
ENST00000697841.1:n.4542C=
ENST00000697842.1:n.3886C=
ENST00000375394.7:c.3631C= MANE Select	ENSP00000364543.2:p.Arg1211=
ENST00000375394.6:c.3631C=	ENSP00000364543.2:p.Arg1211=
ENST00000465703.5:n.4361C=
ENST00000471818.1:n.560C=
ENST00000474839.5:c.*3003C=	ENSP00000420470.1:n.*3003C=
ENST00000483553.5:c.1161C=
ENST00000491994.1:c.720C=
NM_006929.4:c.3631C=	NP_008860.4:p.Arg1211=
XR_926301.3:n.3647C=
NM_006929.5:c.3631C= MANE Select	NP_008860.4:p.Arg1211=