Canonical Allele Identifier: CA2578573576

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969440G>A , CM000668.2:g.31969440G>A	GRCh38
NC_000006.11:g.31937217G>A , CM000668.1:g.31937217G>A	GRCh37
NC_000006.10:g.32045196G>A	NCBI36
NG_032652.1:g.15637G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2514G>A	ENSP00000419905.1:n.*2514G>A
ENST00000483553.6:c.*527G>A	ENSP00000420332.2:n.*527G>A
ENST00000485349.6:n.4016+20G>A
ENST00000491994.2:c.*8G>A	ENSP00000417586.2:n.*8G>A
ENST00000494058.6:n.3842+20G>A
ENST00000697831.1:c.3471+20G>A	ENSP00000513453.1:n.3471+20G>A
ENST00000697832.1:n.3693+20G>A
ENST00000697833.1:c.*488+20G>A	ENSP00000513454.1:n.*488+20G>A
ENST00000697834.1:n.4184G>A
ENST00000697835.1:c.*3058+20G>A	ENSP00000513455.1:n.*3058+20G>A
ENST00000697836.1:n.3871+20G>A
ENST00000697837.1:c.*656+20G>A	ENSP00000513456.1:n.*656+20G>A
ENST00000697838.1:c.3405+20G>A	ENSP00000513457.1:n.3405+20G>A
ENST00000697839.1:n.4278G>A
ENST00000697840.1:c.3576+20G>A	ENSP00000513458.1:n.3576+20G>A
ENST00000697841.1:n.4377G>A
ENST00000697842.1:n.3795+20G>A
ENST00000375394.7:c.3540+20G>A MANE Select	ENSP00000364543.2:n.3540+20G>A
ENST00000375394.6:c.3540+20G>A	ENSP00000364543.2:n.3540+20G>A
ENST00000465703.5:n.4196G>A
ENST00000470453.1:n.383-75G>A
ENST00000471818.1:n.469+20G>A
ENST00000474839.5:c.*2912+20G>A	ENSP00000420470.1:n.*2912+20G>A
ENST00000483553.5:c.996G>A
ENST00000491994.1:c.555G>A
NM_006929.4:c.3540+20G>A	NP_008860.4:n.3540+20G>A
XR_001743586.2:n.3659G>A
XR_926301.3:n.3556+20G>A
NM_006929.5:c.3540+20G>A MANE Select	NP_008860.4:n.3540+20G>A