Canonical Allele Identifier: CA2578573579

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969461G>T , CM000668.2:g.31969461G>T	GRCh38
NC_000006.11:g.31937238G>T , CM000668.1:g.31937238G>T	GRCh37
NC_000006.10:g.32045217G>T	NCBI36
NG_032652.1:g.15658G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2535G>T	ENSP00000419905.1:n.*2535G>T
ENST00000483553.6:c.*548G>T	ENSP00000420332.2:n.*548G>T
ENST00000485349.6:n.4016+41G>T
ENST00000491994.2:c.*29G>T	ENSP00000417586.2:n.*29G>T
ENST00000494058.6:n.3842+41G>T
ENST00000697831.1:c.3471+41G>T	ENSP00000513453.1:n.3471+41G>T
ENST00000697832.1:n.3693+41G>T
ENST00000697833.1:c.*488+41G>T	ENSP00000513454.1:n.*488+41G>T
ENST00000697834.1:n.4205G>T
ENST00000697835.1:c.*3058+41G>T	ENSP00000513455.1:n.*3058+41G>T
ENST00000697836.1:n.3872-31G>T
ENST00000697837.1:c.*656+41G>T	ENSP00000513456.1:n.*656+41G>T
ENST00000697838.1:c.3405+41G>T	ENSP00000513457.1:n.3405+41G>T
ENST00000697839.1:n.4299G>T
ENST00000697840.1:c.3576+41G>T	ENSP00000513458.1:n.3576+41G>T
ENST00000697841.1:n.4398G>T
ENST00000697842.1:n.3795+41G>T
ENST00000375394.7:c.3540+41G>T MANE Select	ENSP00000364543.2:n.3540+41G>T
ENST00000375394.6:c.3540+41G>T	ENSP00000364543.2:n.3540+41G>T
ENST00000465703.5:n.4217G>T
ENST00000470453.1:n.383-54G>T
ENST00000471818.1:n.469+41G>T
ENST00000474839.5:c.*2912+41G>T	ENSP00000420470.1:n.*2912+41G>T
ENST00000483553.5:c.1017G>T
ENST00000491994.1:c.576G>T
NM_006929.4:c.3540+41G>T	NP_008860.4:n.3540+41G>T
XR_001743586.2:n.3680G>T
XR_926301.3:n.3556+41G>T
NM_006929.5:c.3540+41G>T MANE Select	NP_008860.4:n.3540+41G>T