Canonical Allele Identifier: CA363435294
Gene: SKIC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31960221A>C , CM000668.2:g.31960221A>C GRCh38
NC_000006.11:g.31927998A>C , CM000668.1:g.31927998A>C GRCh37
NC_000006.10:g.32035977A>C NCBI36
NG_032652.1:g.6418A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461073.6:c.238A>C ENSP00000419905.1:p.Lys80Gln
ENST00000483553.6:c.238A>C ENSP00000420332.2:p.Lys80Gln
ENST00000485349.6:n.279A>C
ENST00000491994.2:c.238A>C ENSP00000417586.2:p.Lys80Gln
ENST00000494058.6:n.295A>C
ENST00000697831.1:c.238A>C ENSP00000513453.1:p.Lys80Gln
ENST00000697832.1:n.314A>C
ENST00000697833.1:c.238A>C ENSP00000513454.1:p.Lys80Gln
ENST00000697834.1:n.290A>C
ENST00000697835.1:c.257A>C ENSP00000513455.1:p.Lys86Thr
ENST00000697836.1:n.274A>C
ENST00000697837.1:c.238A>C ENSP00000513456.1:p.Lys80Gln
ENST00000697838.1:c.103A>C ENSP00000513457.1:p.Lys35Gln
ENST00000697839.1:n.260A>C
ENST00000697840.1:c.238A>C ENSP00000513458.1:p.Lys80Gln
ENST00000697841.1:n.249A>C
ENST00000697842.1:n.238A>C
ENST00000375394.7:c.238A>C MANE Select ENSP00000364543.2:p.Lys80Gln
ENST00000375394.6:c.238A>C ENSP00000364543.2:p.Lys80Gln
ENST00000461073.5:c.238A>C ENSP00000419905.1:p.Lys80Gln
ENST00000465703.5:n.290A>C
ENST00000474839.5:c.127-820A>C ENSP00000420470.1:n.127-820A>C
ENST00000488648.5:n.314A>C
ENST00000628157.1:c.127-820A>C ENSP00000485707.1:n.127-820A>C
NM_006929.4:c.238A>C NP_008860.4:p.Lys80Gln
XM_006715168.2:c.238A>C XP_006715231.1:p.Lys80Gln
XM_011514815.1:c.238A>C XP_011513117.1:p.Lys80Gln
XR_926301.1:n.326A>C
XM_011514815.3:c.238A>C XP_011513117.1:p.Lys80Gln
XR_001743586.2:n.274A>C
XR_926301.3:n.274A>C
NM_006929.5:c.238A>C MANE Select NP_008860.4:p.Lys80Gln