Canonical Allele Identifier: CA1619377251

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960191G= , CM000668.2:g.31960191G=	GRCh38
NC_000006.11:g.31927968G= , CM000668.1:g.31927968G=	GRCh37
NC_000006.10:g.32035947G=	NCBI36
NG_032652.1:g.6388G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.237-29G=	ENSP00000419905.1:n.237-29G=
ENST00000483553.6:c.237-29G=	ENSP00000420332.2:n.237-29G=
ENST00000485349.6:n.278-29G=
ENST00000491994.2:c.237-29G=	ENSP00000417586.2:n.237-29G=
ENST00000494058.6:n.294-29G=
ENST00000697831.1:c.237-29G=	ENSP00000513453.1:n.237-29G=
ENST00000697832.1:n.313-29G=
ENST00000697833.1:c.237-29G=	ENSP00000513454.1:n.237-29G=
ENST00000697834.1:n.289-29G=
ENST00000697835.1:c.237-10G=	ENSP00000513455.1:n.237-10G=
ENST00000697836.1:n.273-29G=
ENST00000697837.1:c.237-29G=	ENSP00000513456.1:n.237-29G=
ENST00000697838.1:c.102-29G=	ENSP00000513457.1:n.102-29G=
ENST00000697839.1:n.259-29G=
ENST00000697840.1:c.237-29G=	ENSP00000513458.1:n.237-29G=
ENST00000697841.1:n.248-29G=
ENST00000697842.1:n.237-29G=
ENST00000375394.7:c.237-29G= MANE Select	ENSP00000364543.2:n.237-29G=
ENST00000375394.6:c.237-29G=	ENSP00000364543.2:n.237-29G=
ENST00000461073.5:c.237-29G=	ENSP00000419905.1:n.237-29G=
ENST00000465703.5:n.289-29G=
ENST00000474839.5:c.126+791G=	ENSP00000420470.1:n.126+791G=
ENST00000488648.5:n.313-29G=
ENST00000628157.1:c.126+791G=	ENSP00000485707.1:n.126+791G=
NM_006929.4:c.237-29G=	NP_008860.4:n.237-29G=
XM_006715168.2:c.237-29G=	XP_006715231.1:n.237-29G=
XM_011514815.1:c.237-29G=	XP_011513117.1:n.237-29G=
XR_926301.1:n.325-29G=
XM_011514815.3:c.237-29G=	XP_011513117.1:n.237-29G=
XR_001743586.2:n.273-29G=
XR_926301.3:n.273-29G=
NM_006929.5:c.237-29G= MANE Select	NP_008860.4:n.237-29G=