Canonical Allele Identifier: CA2711459785

Gene: SKIC2

Linked Data

• dbSNP Id: rs2151817811

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969468C>T , CM000668.2:g.31969468C>T	GRCh38
NC_000006.11:g.31937245C>T , CM000668.1:g.31937245C>T	GRCh37
NC_000006.10:g.32045224C>T	NCBI36
NG_032652.1:g.15665C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2542C>T	ENSP00000419905.1:n.*2542C>T
ENST00000483553.6:c.*555C>T	ENSP00000420332.2:n.*555C>T
ENST00000485349.6:n.4017-47C>T
ENST00000491994.2:c.*36C>T	ENSP00000417586.2:n.*36C>T
ENST00000494058.6:n.3843-47C>T
ENST00000697831.1:c.3472-47C>T	ENSP00000513453.1:n.3472-47C>T
ENST00000697832.1:n.3694-47C>T
ENST00000697833.1:c.*489-47C>T	ENSP00000513454.1:n.*489-47C>T
ENST00000697834.1:n.4212C>T
ENST00000697835.1:c.*3059-47C>T	ENSP00000513455.1:n.*3059-47C>T
ENST00000697836.1:n.3872-24C>T
ENST00000697837.1:c.*657-47C>T	ENSP00000513456.1:n.*657-47C>T
ENST00000697838.1:c.3406-47C>T	ENSP00000513457.1:n.3406-47C>T
ENST00000697839.1:n.4306C>T
ENST00000697840.1:c.3577-47C>T	ENSP00000513458.1:n.3577-47C>T
ENST00000697841.1:n.4405C>T
ENST00000697842.1:n.3796-47C>T
ENST00000375394.7:c.3541-47C>T MANE Select	ENSP00000364543.2:n.3541-47C>T
ENST00000375394.6:c.3541-47C>T	ENSP00000364543.2:n.3541-47C>T
ENST00000465703.5:n.4224C>T
ENST00000470453.1:n.383-47C>T
ENST00000471818.1:n.470-47C>T
ENST00000474839.5:c.*2913-47C>T	ENSP00000420470.1:n.*2913-47C>T
ENST00000483553.5:c.1024C>T
ENST00000491994.1:c.583C>T
NM_006929.4:c.3541-47C>T	NP_008860.4:n.3541-47C>T
XR_001743586.2:n.3687C>T
XR_926301.3:n.3557-47C>T
NM_006929.5:c.3541-47C>T MANE Select	NP_008860.4:n.3541-47C>T