Canonical Allele Identifier: CA1619377360

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960272_31960274delinsCCA , CM000668.2:g.31960272_31960274delinsCCA	GRCh38
NC_000006.11:g.31928049_31928051delinsCCA , CM000668.1:g.31928049_31928051delinsCCA	GRCh37
NC_000006.10:g.32036028_32036030delinsCCA	NCBI36
NG_032652.1:g.6469_6471delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.289_291delinsCCA	ENSP00000419905.1:p.Pro97=
ENST00000483553.6:c.289_291delinsCCA	ENSP00000420332.2:p.Pro97=
ENST00000485349.6:n.330_332delinsCCA
ENST00000491994.2:c.289_291delinsCCA	ENSP00000417586.2:p.Pro97=
ENST00000494058.6:n.346_348delinsCCA
ENST00000697831.1:c.289_291delinsCCA	ENSP00000513453.1:p.Pro97=
ENST00000697832.1:n.365_367delinsCCA
ENST00000697833.1:c.289_291delinsCCA	ENSP00000513454.1:p.Pro97=
ENST00000697834.1:n.341_343delinsCCA
ENST00000697835.1:c.308_310delinsCCA	ENSP00000513455.1:p.Pro103=
ENST00000697836.1:n.325_327delinsCCA
ENST00000697837.1:c.289_291delinsCCA	ENSP00000513456.1:p.Pro97=
ENST00000697838.1:c.154_156delinsCCA	ENSP00000513457.1:p.Pro52=
ENST00000697839.1:n.311_313delinsCCA
ENST00000697840.1:c.289_291delinsCCA	ENSP00000513458.1:p.Pro97=
ENST00000697841.1:n.300_302delinsCCA
ENST00000697842.1:n.289_291delinsCCA
ENST00000375394.7:c.289_291delinsCCA MANE Select	ENSP00000364543.2:p.Pro97=
ENST00000375394.6:c.289_291delinsCCA	ENSP00000364543.2:p.Pro97=
ENST00000461073.5:c.289_291delinsCCA	ENSP00000419905.1:p.Pro97=
ENST00000465703.5:n.341_343delinsCCA
ENST00000474839.5:c.127-769_127-767delinsCCA	ENSP00000420470.1:n.127-769_127-767delinsCCA
ENST00000488648.5:n.365_367delinsCCA
ENST00000628157.1:c.127-769_127-767delinsCCA	ENSP00000485707.1:n.127-769_127-767delinsCCA
NM_006929.4:c.289_291delinsCCA	NP_008860.4:p.Pro97=
XM_006715168.2:c.289_291delinsCCA	XP_006715231.1:p.Pro97=
XM_011514815.1:c.289_291delinsCCA	XP_011513117.1:p.Pro97=
XR_926301.1:n.377_379delinsCCA
XM_011514815.3:c.289_291delinsCCA	XP_011513117.1:p.Pro97=
XR_001743586.2:n.325_327delinsCCA
XR_926301.3:n.325_327delinsCCA
NM_006929.5:c.289_291delinsCCA MANE Select	NP_008860.4:p.Pro97=