Canonical Allele Identifier: CA1619384398

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969560G= , CM000668.2:g.31969560G=	GRCh38
NC_000006.11:g.31937337G= , CM000668.1:g.31937337G=	GRCh37
NC_000006.10:g.32045316G=	NCBI36
NG_032652.1:g.15757G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2634G=	ENSP00000419905.1:n.*2634G=
ENST00000485349.6:n.4062G=
ENST00000491994.2:c.*128G=	ENSP00000417586.2:n.*128G=
ENST00000494058.6:n.3888G=
ENST00000697831.1:c.3517G=	ENSP00000513453.1:p.Val1173=
ENST00000697832.1:n.3739G=
ENST00000697833.1:c.*534G=	ENSP00000513454.1:n.*534G=
ENST00000697834.1:n.4304G=
ENST00000697835.1:c.*3104G=	ENSP00000513455.1:n.*3104G=
ENST00000697836.1:n.3940G=
ENST00000697837.1:c.*702G=	ENSP00000513456.1:n.*702G=
ENST00000697838.1:c.3451G=	ENSP00000513457.1:p.Val1151=
ENST00000697839.1:n.4398G=
ENST00000697840.1:c.3622G=	ENSP00000513458.1:p.Val1208=
ENST00000697841.1:n.4497G=
ENST00000697842.1:n.3841G=
ENST00000375394.7:c.3586G= MANE Select	ENSP00000364543.2:p.Val1196=
ENST00000375394.6:c.3586G=	ENSP00000364543.2:p.Val1196=
ENST00000465703.5:n.4316G=
ENST00000470453.1:n.428G=
ENST00000471818.1:n.515G=
ENST00000474839.5:c.*2958G=	ENSP00000420470.1:n.*2958G=
ENST00000483553.5:c.1116G=
ENST00000491994.1:c.675G=
NM_006929.4:c.3586G=	NP_008860.4:p.Val1196=
XR_926301.3:n.3602G=
NM_006929.5:c.3586G= MANE Select	NP_008860.4:p.Val1196=