Canonical Allele Identifier: CA1619384399

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969563G= , CM000668.2:g.31969563G=	GRCh38
NC_000006.11:g.31937340G= , CM000668.1:g.31937340G=	GRCh37
NC_000006.10:g.32045319G=	NCBI36
NG_032652.1:g.15760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2637G=	ENSP00000419905.1:n.*2637G=
ENST00000485349.6:n.4065G=
ENST00000491994.2:c.*131G=	ENSP00000417586.2:n.*131G=
ENST00000494058.6:n.3891G=
ENST00000697831.1:c.3520G=	ENSP00000513453.1:p.Val1174=
ENST00000697832.1:n.3742G=
ENST00000697833.1:c.*537G=	ENSP00000513454.1:n.*537G=
ENST00000697834.1:n.4307G=
ENST00000697835.1:c.*3107G=	ENSP00000513455.1:n.*3107G=
ENST00000697836.1:n.3943G=
ENST00000697837.1:c.*705G=	ENSP00000513456.1:n.*705G=
ENST00000697838.1:c.3454G=	ENSP00000513457.1:p.Val1152=
ENST00000697839.1:n.4401G=
ENST00000697840.1:c.3625G=	ENSP00000513458.1:p.Val1209=
ENST00000697841.1:n.4500G=
ENST00000697842.1:n.3844G=
ENST00000375394.7:c.3589G= MANE Select	ENSP00000364543.2:p.Val1197=
ENST00000375394.6:c.3589G=	ENSP00000364543.2:p.Val1197=
ENST00000465703.5:n.4319G=
ENST00000470453.1:n.431G=
ENST00000471818.1:n.518G=
ENST00000474839.5:c.*2961G=	ENSP00000420470.1:n.*2961G=
ENST00000483553.5:c.1119G=
ENST00000491994.1:c.678G=
NM_006929.4:c.3589G=	NP_008860.4:p.Val1197=
XR_926301.3:n.3605G=
NM_006929.5:c.3589G= MANE Select	NP_008860.4:p.Val1197=