Canonical Allele Identifier: CA1619384354

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969439G= , CM000668.2:g.31969439G=	GRCh38
NC_000006.11:g.31937216G= , CM000668.1:g.31937216G=	GRCh37
NC_000006.10:g.32045195G=	NCBI36
NG_032652.1:g.15636G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2513G=	ENSP00000419905.1:n.*2513G=
ENST00000483553.6:c.*526G=	ENSP00000420332.2:n.*526G=
ENST00000485349.6:n.4016+19G=
ENST00000491994.2:c.*7G=	ENSP00000417586.2:n.*7G=
ENST00000494058.6:n.3842+19G=
ENST00000697831.1:c.3471+19G=	ENSP00000513453.1:n.3471+19G=
ENST00000697832.1:n.3693+19G=
ENST00000697833.1:c.*488+19G=	ENSP00000513454.1:n.*488+19G=
ENST00000697834.1:n.4183G=
ENST00000697835.1:c.*3058+19G=	ENSP00000513455.1:n.*3058+19G=
ENST00000697836.1:n.3871+19G=
ENST00000697837.1:c.*656+19G=	ENSP00000513456.1:n.*656+19G=
ENST00000697838.1:c.3405+19G=	ENSP00000513457.1:n.3405+19G=
ENST00000697839.1:n.4277G=
ENST00000697840.1:c.3576+19G=	ENSP00000513458.1:n.3576+19G=
ENST00000697841.1:n.4376G=
ENST00000697842.1:n.3795+19G=
ENST00000375394.7:c.3540+19G= MANE Select	ENSP00000364543.2:n.3540+19G=
ENST00000375394.6:c.3540+19G=	ENSP00000364543.2:n.3540+19G=
ENST00000465703.5:n.4195G=
ENST00000470453.1:n.383-76G=
ENST00000471818.1:n.469+19G=
ENST00000474839.5:c.*2912+19G=	ENSP00000420470.1:n.*2912+19G=
ENST00000483553.5:c.995G=
ENST00000491994.1:c.554G=
NM_006929.4:c.3540+19G=	NP_008860.4:n.3540+19G=
XR_001743586.2:n.3658G=
XR_926301.3:n.3556+19G=
NM_006929.5:c.3540+19G= MANE Select	NP_008860.4:n.3540+19G=