Canonical Allele Identifier: CA1087496342

Gene: SKIC2

Linked Data

• dbSNP Id: rs1772385889
• gnomAD v3: 6-31960206-AT-A
• gnomAD v4: 6-31960206-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960211del , CM000668.2:g.31960211del	GRCh38
NC_000006.11:g.31927988del , CM000668.1:g.31927988del	GRCh37
NC_000006.10:g.32035967del	NCBI36
NG_032652.1:g.6408del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.237-9del	ENSP00000419905.1:n.237-9del
ENST00000483553.6:c.237-9del	ENSP00000420332.2:n.237-9del
ENST00000485349.6:n.278-9del
ENST00000491994.2:c.237-9del	ENSP00000417586.2:n.237-9del
ENST00000494058.6:n.294-9del
ENST00000697831.1:c.237-9del	ENSP00000513453.1:n.237-9del
ENST00000697832.1:n.313-9del
ENST00000697833.1:c.237-9del	ENSP00000513454.1:n.237-9del
ENST00000697834.1:n.289-9del
ENST00000697835.1:c.247del	ENSP00000513455.1:p.Ser83LeufsTer?
ENST00000697836.1:n.273-9del
ENST00000697837.1:c.237-9del	ENSP00000513456.1:n.237-9del
ENST00000697838.1:c.102-9del	ENSP00000513457.1:n.102-9del
ENST00000697839.1:n.259-9del
ENST00000697840.1:c.237-9del	ENSP00000513458.1:n.237-9del
ENST00000697841.1:n.248-9del
ENST00000697842.1:n.237-9del
ENST00000375394.7:c.237-9del MANE Select	ENSP00000364543.2:n.237-9del
ENST00000375394.6:c.237-9del	ENSP00000364543.2:n.237-9del
ENST00000461073.5:c.237-9del	ENSP00000419905.1:n.237-9del
ENST00000465703.5:n.289-9del
ENST00000474839.5:c.126+811del	ENSP00000420470.1:n.126+811del
ENST00000488648.5:n.313-9del
ENST00000628157.1:c.126+811del	ENSP00000485707.1:n.126+811del
NM_006929.4:c.237-9del	NP_008860.4:n.237-9del
XM_006715168.2:c.237-9del	XP_006715231.1:n.237-9del
XM_011514815.1:c.237-9del	XP_011513117.1:n.237-9del
XR_926301.1:n.325-9del
XM_011514815.3:c.237-9del	XP_011513117.1:n.237-9del
XR_001743586.2:n.273-9del
XR_926301.3:n.273-9del
NM_006929.5:c.237-9del MANE Select	NP_008860.4:n.237-9del