Canonical Allele Identifier: CA1619384366

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969476G= , CM000668.2:g.31969476G=	GRCh38
NC_000006.11:g.31937253G= , CM000668.1:g.31937253G=	GRCh37
NC_000006.10:g.32045232G=	NCBI36
NG_032652.1:g.15673G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2550G=	ENSP00000419905.1:n.*2550G=
ENST00000483553.6:c.*563G=	ENSP00000420332.2:n.*563G=
ENST00000485349.6:n.4017-39G=
ENST00000491994.2:c.*44G=	ENSP00000417586.2:n.*44G=
ENST00000494058.6:n.3843-39G=
ENST00000697831.1:c.3472-39G=	ENSP00000513453.1:n.3472-39G=
ENST00000697832.1:n.3694-39G=
ENST00000697833.1:c.*489-39G=	ENSP00000513454.1:n.*489-39G=
ENST00000697834.1:n.4220G=
ENST00000697835.1:c.*3059-39G=	ENSP00000513455.1:n.*3059-39G=
ENST00000697836.1:n.3872-16G=
ENST00000697837.1:c.*657-39G=	ENSP00000513456.1:n.*657-39G=
ENST00000697838.1:c.3406-39G=	ENSP00000513457.1:n.3406-39G=
ENST00000697839.1:n.4314G=
ENST00000697840.1:c.3577-39G=	ENSP00000513458.1:n.3577-39G=
ENST00000697841.1:n.4413G=
ENST00000697842.1:n.3796-39G=
ENST00000375394.7:c.3541-39G= MANE Select	ENSP00000364543.2:n.3541-39G=
ENST00000375394.6:c.3541-39G=	ENSP00000364543.2:n.3541-39G=
ENST00000465703.5:n.4232G=
ENST00000470453.1:n.383-39G=
ENST00000471818.1:n.470-39G=
ENST00000474839.5:c.*2913-39G=	ENSP00000420470.1:n.*2913-39G=
ENST00000483553.5:c.1032G=
ENST00000491994.1:c.591G=
NM_006929.4:c.3541-39G=	NP_008860.4:n.3541-39G=
XR_001743586.2:n.3695G=
XR_926301.3:n.3557-39G=
NM_006929.5:c.3541-39G= MANE Select	NP_008860.4:n.3541-39G=