Canonical Allele Identifier: CA1619384323

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969365T= , CM000668.2:g.31969365T=	GRCh38
NC_000006.11:g.31937142T= , CM000668.1:g.31937142T=	GRCh37
NC_000006.10:g.32045121T=	NCBI36
NG_032652.1:g.15562T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2439T=	ENSP00000419905.1:n.*2439T=
ENST00000483553.6:c.*452T=	ENSP00000420332.2:n.*452T=
ENST00000485349.6:n.3961T=
ENST00000491994.2:c.3485T=	ENSP00000417586.2:p.Val1162=
ENST00000494058.6:n.3787T=
ENST00000697831.1:c.3416T=	ENSP00000513453.1:p.Val1139=
ENST00000697832.1:n.3638T=
ENST00000697833.1:c.*433T=	ENSP00000513454.1:n.*433T=
ENST00000697834.1:n.4109T=
ENST00000697835.1:c.*3003T=	ENSP00000513455.1:n.*3003T=
ENST00000697836.1:n.3816T=
ENST00000697837.1:c.*601T=	ENSP00000513456.1:n.*601T=
ENST00000697838.1:c.3350T=	ENSP00000513457.1:p.Val1117=
ENST00000697839.1:n.4203T=
ENST00000697840.1:c.3521T=	ENSP00000513458.1:p.Val1174=
ENST00000697841.1:n.4302T=
ENST00000697842.1:n.3740T=
ENST00000375394.7:c.3485T= MANE Select	ENSP00000364543.2:p.Val1162=
ENST00000375394.6:c.3485T=	ENSP00000364543.2:p.Val1162=
ENST00000465703.5:n.4121T=
ENST00000470453.1:n.382+49T=
ENST00000471818.1:n.414T=
ENST00000474839.5:c.*2857T=	ENSP00000420470.1:n.*2857T=
ENST00000483553.5:c.921T=
ENST00000485349.5:n.691T=
ENST00000491994.1:c.480T=
NM_006929.4:c.3485T=	NP_008860.4:p.Val1162=
XR_001743586.2:n.3584T=
XR_926301.3:n.3501T=
NM_006929.5:c.3485T= MANE Select	NP_008860.4:p.Val1162=