Canonical Allele Identifier: CA1619384379

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969502A= , CM000668.2:g.31969502A=	GRCh38
NC_000006.11:g.31937279A= , CM000668.1:g.31937279A=	GRCh37
NC_000006.10:g.32045258A=	NCBI36
NG_032652.1:g.15699A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2576A=	ENSP00000419905.1:n.*2576A=
ENST00000485349.6:n.4017-13A=
ENST00000491994.2:c.*70A=	ENSP00000417586.2:n.*70A=
ENST00000494058.6:n.3843-13A=
ENST00000697831.1:c.3472-13A=	ENSP00000513453.1:n.3472-13A=
ENST00000697832.1:n.3694-13A=
ENST00000697833.1:c.*489-13A=	ENSP00000513454.1:n.*489-13A=
ENST00000697834.1:n.4246A=
ENST00000697835.1:c.*3059-13A=	ENSP00000513455.1:n.*3059-13A=
ENST00000697836.1:n.3882A=
ENST00000697837.1:c.*657-13A=	ENSP00000513456.1:n.*657-13A=
ENST00000697838.1:c.3406-13A=	ENSP00000513457.1:n.3406-13A=
ENST00000697839.1:n.4340A=
ENST00000697840.1:c.3577-13A=	ENSP00000513458.1:n.3577-13A=
ENST00000697841.1:n.4439A=
ENST00000697842.1:n.3796-13A=
ENST00000375394.7:c.3541-13A= MANE Select	ENSP00000364543.2:n.3541-13A=
ENST00000375394.6:c.3541-13A=	ENSP00000364543.2:n.3541-13A=
ENST00000465703.5:n.4258A=
ENST00000470453.1:n.383-13A=
ENST00000471818.1:n.470-13A=
ENST00000474839.5:c.*2913-13A=	ENSP00000420470.1:n.*2913-13A=
ENST00000483553.5:c.1058A=
ENST00000491994.1:c.617A=
NM_006929.4:c.3541-13A=	NP_008860.4:n.3541-13A=
XR_926301.3:n.3557-13A=
NM_006929.5:c.3541-13A= MANE Select	NP_008860.4:n.3541-13A=