Canonical Allele Identifier: CA363490297
Gene: SKIC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31969403G>A , CM000668.2:g.31969403G>A GRCh38
NC_000006.11:g.31937180G>A , CM000668.1:g.31937180G>A GRCh37
NC_000006.10:g.32045159G>A NCBI36
NG_032652.1:g.15600G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461073.6:c.*2477G>A ENSP00000419905.1:n.*2477G>A
ENST00000483553.6:c.*490G>A ENSP00000420332.2:n.*490G>A
ENST00000485349.6:n.3999G>A
ENST00000491994.2:c.3523G>A ENSP00000417586.2:p.Glu1175Lys
ENST00000494058.6:n.3825G>A
ENST00000697831.1:c.3454G>A ENSP00000513453.1:p.Glu1152Lys
ENST00000697832.1:n.3676G>A
ENST00000697833.1:c.*471G>A ENSP00000513454.1:n.*471G>A
ENST00000697834.1:n.4147G>A
ENST00000697835.1:c.*3041G>A ENSP00000513455.1:n.*3041G>A
ENST00000697836.1:n.3854G>A
ENST00000697837.1:c.*639G>A ENSP00000513456.1:n.*639G>A
ENST00000697838.1:c.3388G>A ENSP00000513457.1:p.Glu1130Lys
ENST00000697839.1:n.4241G>A
ENST00000697840.1:c.3559G>A ENSP00000513458.1:p.Glu1187Lys
ENST00000697841.1:n.4340G>A
ENST00000697842.1:n.3778G>A
ENST00000375394.7:c.3523G>A MANE Select ENSP00000364543.2:p.Glu1175Lys
ENST00000375394.6:c.3523G>A ENSP00000364543.2:p.Glu1175Lys
ENST00000465703.5:n.4159G>A
ENST00000470453.1:n.382+87G>A
ENST00000471818.1:n.452G>A
ENST00000474839.5:c.*2895G>A ENSP00000420470.1:n.*2895G>A
ENST00000483553.5:c.959G>A
ENST00000485349.5:n.729G>A
ENST00000491994.1:c.518G>A
NM_006929.4:c.3523G>A NP_008860.4:p.Glu1175Lys
XR_001743586.2:n.3622G>A
XR_926301.3:n.3539G>A
NM_006929.5:c.3523G>A MANE Select NP_008860.4:p.Glu1175Lys