Canonical Allele Identifier: CA2578573094

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960184_31960186del , CM000668.2:g.31960184_31960186del	GRCh38
NC_000006.11:g.31927961_31927963del , CM000668.1:g.31927961_31927963del	GRCh37
NC_000006.10:g.32035940_32035942del	NCBI36
NG_032652.1:g.6381_6383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.237-36_237-34del	ENSP00000419905.1:n.237-36_237-34del
ENST00000483553.6:c.237-36_237-34del	ENSP00000420332.2:n.237-36_237-34del
ENST00000485349.6:n.278-36_278-34del
ENST00000491994.2:c.237-36_237-34del	ENSP00000417586.2:n.237-36_237-34del
ENST00000494058.6:n.294-36_294-34del
ENST00000697831.1:c.237-36_237-34del	ENSP00000513453.1:n.237-36_237-34del
ENST00000697832.1:n.313-36_313-34del
ENST00000697833.1:c.237-36_237-34del	ENSP00000513454.1:n.237-36_237-34del
ENST00000697834.1:n.289-36_289-34del
ENST00000697835.1:c.237-17_237-15del	ENSP00000513455.1:n.237-17_237-15del
ENST00000697836.1:n.273-36_273-34del
ENST00000697837.1:c.237-36_237-34del	ENSP00000513456.1:n.237-36_237-34del
ENST00000697838.1:c.102-36_102-34del	ENSP00000513457.1:n.102-36_102-34del
ENST00000697839.1:n.259-36_259-34del
ENST00000697840.1:c.237-36_237-34del	ENSP00000513458.1:n.237-36_237-34del
ENST00000697841.1:n.248-36_248-34del
ENST00000697842.1:n.237-36_237-34del
ENST00000375394.7:c.237-36_237-34del MANE Select	ENSP00000364543.2:n.237-36_237-34del
ENST00000375394.6:c.237-36_237-34del	ENSP00000364543.2:n.237-36_237-34del
ENST00000461073.5:c.237-36_237-34del	ENSP00000419905.1:n.237-36_237-34del
ENST00000465703.5:n.289-36_289-34del
ENST00000474839.5:c.126+784_126+786del	ENSP00000420470.1:n.126+784_126+786del
ENST00000488648.5:n.313-36_313-34del
ENST00000628157.1:c.126+784_126+786del	ENSP00000485707.1:n.126+784_126+786del
NM_006929.4:c.237-36_237-34del	NP_008860.4:n.237-36_237-34del
XM_006715168.2:c.237-36_237-34del	XP_006715231.1:n.237-36_237-34del
XM_011514815.1:c.237-36_237-34del	XP_011513117.1:n.237-36_237-34del
XR_926301.1:n.325-36_325-34del
XM_011514815.3:c.237-36_237-34del	XP_011513117.1:n.237-36_237-34del
XR_001743586.2:n.273-36_273-34del
XR_926301.3:n.273-36_273-34del
NM_006929.5:c.237-36_237-34del MANE Select	NP_008860.4:n.237-36_237-34del