Canonical Allele Identifier: CA1619384374

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969485C= , CM000668.2:g.31969485C=	GRCh38
NC_000006.11:g.31937262C= , CM000668.1:g.31937262C=	GRCh37
NC_000006.10:g.32045241C=	NCBI36
NG_032652.1:g.15682C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2559C=	ENSP00000419905.1:n.*2559C=
ENST00000483553.6:c.*572C=	ENSP00000420332.2:n.*572C=
ENST00000485349.6:n.4017-30C=
ENST00000491994.2:c.*53C=	ENSP00000417586.2:n.*53C=
ENST00000494058.6:n.3843-30C=
ENST00000697831.1:c.3472-30C=	ENSP00000513453.1:n.3472-30C=
ENST00000697832.1:n.3694-30C=
ENST00000697833.1:c.*489-30C=	ENSP00000513454.1:n.*489-30C=
ENST00000697834.1:n.4229C=
ENST00000697835.1:c.*3059-30C=	ENSP00000513455.1:n.*3059-30C=
ENST00000697836.1:n.3872-7C=
ENST00000697837.1:c.*657-30C=	ENSP00000513456.1:n.*657-30C=
ENST00000697838.1:c.3406-30C=	ENSP00000513457.1:n.3406-30C=
ENST00000697839.1:n.4323C=
ENST00000697840.1:c.3577-30C=	ENSP00000513458.1:n.3577-30C=
ENST00000697841.1:n.4422C=
ENST00000697842.1:n.3796-30C=
ENST00000375394.7:c.3541-30C= MANE Select	ENSP00000364543.2:n.3541-30C=
ENST00000375394.6:c.3541-30C=	ENSP00000364543.2:n.3541-30C=
ENST00000465703.5:n.4241C=
ENST00000470453.1:n.383-30C=
ENST00000471818.1:n.470-30C=
ENST00000474839.5:c.*2913-30C=	ENSP00000420470.1:n.*2913-30C=
ENST00000483553.5:c.1041C=
ENST00000491994.1:c.600C=
NM_006929.4:c.3541-30C=	NP_008860.4:n.3541-30C=
XR_001743586.2:n.3704C=
XR_926301.3:n.3557-30C=
NM_006929.5:c.3541-30C= MANE Select	NP_008860.4:n.3541-30C=