Canonical Allele Identifier: CA1619384368

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969478C= , CM000668.2:g.31969478C=	GRCh38
NC_000006.11:g.31937255C= , CM000668.1:g.31937255C=	GRCh37
NC_000006.10:g.32045234C=	NCBI36
NG_032652.1:g.15675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2552C=	ENSP00000419905.1:n.*2552C=
ENST00000483553.6:c.*565C=	ENSP00000420332.2:n.*565C=
ENST00000485349.6:n.4017-37C=
ENST00000491994.2:c.*46C=	ENSP00000417586.2:n.*46C=
ENST00000494058.6:n.3843-37C=
ENST00000697831.1:c.3472-37C=	ENSP00000513453.1:n.3472-37C=
ENST00000697832.1:n.3694-37C=
ENST00000697833.1:c.*489-37C=	ENSP00000513454.1:n.*489-37C=
ENST00000697834.1:n.4222C=
ENST00000697835.1:c.*3059-37C=	ENSP00000513455.1:n.*3059-37C=
ENST00000697836.1:n.3872-14C=
ENST00000697837.1:c.*657-37C=	ENSP00000513456.1:n.*657-37C=
ENST00000697838.1:c.3406-37C=	ENSP00000513457.1:n.3406-37C=
ENST00000697839.1:n.4316C=
ENST00000697840.1:c.3577-37C=	ENSP00000513458.1:n.3577-37C=
ENST00000697841.1:n.4415C=
ENST00000697842.1:n.3796-37C=
ENST00000375394.7:c.3541-37C= MANE Select	ENSP00000364543.2:n.3541-37C=
ENST00000375394.6:c.3541-37C=	ENSP00000364543.2:n.3541-37C=
ENST00000465703.5:n.4234C=
ENST00000470453.1:n.383-37C=
ENST00000471818.1:n.470-37C=
ENST00000474839.5:c.*2913-37C=	ENSP00000420470.1:n.*2913-37C=
ENST00000483553.5:c.1034C=
ENST00000491994.1:c.593C=
NM_006929.4:c.3541-37C=	NP_008860.4:n.3541-37C=
XR_001743586.2:n.3697C=
XR_926301.3:n.3557-37C=
NM_006929.5:c.3541-37C= MANE Select	NP_008860.4:n.3541-37C=