Canonical Allele Identifier: CA1619384376

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969489C= , CM000668.2:g.31969489C=	GRCh38
NC_000006.11:g.31937266C= , CM000668.1:g.31937266C=	GRCh37
NC_000006.10:g.32045245C=	NCBI36
NG_032652.1:g.15686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2563C=	ENSP00000419905.1:n.*2563C=
ENST00000483553.6:c.*576C=	ENSP00000420332.2:n.*576C=
ENST00000485349.6:n.4017-26C=
ENST00000491994.2:c.*57C=	ENSP00000417586.2:n.*57C=
ENST00000494058.6:n.3843-26C=
ENST00000697831.1:c.3472-26C=	ENSP00000513453.1:n.3472-26C=
ENST00000697832.1:n.3694-26C=
ENST00000697833.1:c.*489-26C=	ENSP00000513454.1:n.*489-26C=
ENST00000697834.1:n.4233C=
ENST00000697835.1:c.*3059-26C=	ENSP00000513455.1:n.*3059-26C=
ENST00000697836.1:n.3872-3C=
ENST00000697837.1:c.*657-26C=	ENSP00000513456.1:n.*657-26C=
ENST00000697838.1:c.3406-26C=	ENSP00000513457.1:n.3406-26C=
ENST00000697839.1:n.4327C=
ENST00000697840.1:c.3577-26C=	ENSP00000513458.1:n.3577-26C=
ENST00000697841.1:n.4426C=
ENST00000697842.1:n.3796-26C=
ENST00000375394.7:c.3541-26C= MANE Select	ENSP00000364543.2:n.3541-26C=
ENST00000375394.6:c.3541-26C=	ENSP00000364543.2:n.3541-26C=
ENST00000465703.5:n.4245C=
ENST00000470453.1:n.383-26C=
ENST00000471818.1:n.470-26C=
ENST00000474839.5:c.*2913-26C=	ENSP00000420470.1:n.*2913-26C=
ENST00000483553.5:c.1045C=
ENST00000491994.1:c.604C=
NM_006929.4:c.3541-26C=	NP_008860.4:n.3541-26C=
XR_001743586.2:n.3708C=
XR_926301.3:n.3557-26C=
NM_006929.5:c.3541-26C= MANE Select	NP_008860.4:n.3541-26C=