Canonical Allele Identifier: CA2739912271

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969424A>G , CM000668.2:g.31969424A>G	GRCh38
NC_000006.11:g.31937201A>G , CM000668.1:g.31937201A>G	GRCh37
NC_000006.10:g.32045180A>G	NCBI36
NG_032652.1:g.15621A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2498A>G	ENSP00000419905.1:n.*2498A>G
ENST00000483553.6:c.*511A>G	ENSP00000420332.2:n.*511A>G
ENST00000485349.6:n.4016+4A>G
ENST00000491994.2:c.3544A>G	ENSP00000417586.2:p.Ser1182Gly
ENST00000494058.6:n.3842+4A>G
ENST00000697831.1:c.3471+4A>G	ENSP00000513453.1:n.3471+4A>G
ENST00000697832.1:n.3693+4A>G
ENST00000697833.1:c.*488+4A>G	ENSP00000513454.1:n.*488+4A>G
ENST00000697834.1:n.4168A>G
ENST00000697835.1:c.*3058+4A>G	ENSP00000513455.1:n.*3058+4A>G
ENST00000697836.1:n.3871+4A>G
ENST00000697837.1:c.*656+4A>G	ENSP00000513456.1:n.*656+4A>G
ENST00000697838.1:c.3405+4A>G	ENSP00000513457.1:n.3405+4A>G
ENST00000697839.1:n.4262A>G
ENST00000697840.1:c.3576+4A>G	ENSP00000513458.1:n.3576+4A>G
ENST00000697841.1:n.4361A>G
ENST00000697842.1:n.3795+4A>G
ENST00000375394.7:c.3540+4A>G MANE Select	ENSP00000364543.2:n.3540+4A>G
ENST00000375394.6:c.3540+4A>G	ENSP00000364543.2:n.3540+4A>G
ENST00000465703.5:n.4180A>G
ENST00000470453.1:n.383-91A>G
ENST00000471818.1:n.469+4A>G
ENST00000474839.5:c.*2912+4A>G	ENSP00000420470.1:n.*2912+4A>G
ENST00000483553.5:c.980A>G
ENST00000491994.1:c.539A>G
NM_006929.4:c.3540+4A>G	NP_008860.4:n.3540+4A>G
XR_001743586.2:n.3643A>G
XR_926301.3:n.3556+4A>G
NM_006929.5:c.3540+4A>G MANE Select	NP_008860.4:n.3540+4A>G