Canonical Allele Identifier: CA1619384307

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969337G= , CM000668.2:g.31969337G=	GRCh38
NC_000006.11:g.31937114G= , CM000668.1:g.31937114G=	GRCh37
NC_000006.10:g.32045093G=	NCBI36
NG_032652.1:g.15534G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2411G=	ENSP00000419905.1:n.*2411G=
ENST00000483553.6:c.*424G=	ENSP00000420332.2:n.*424G=
ENST00000485349.6:n.3933G=
ENST00000491994.2:c.3457G=	ENSP00000417586.2:p.Gly1153=
ENST00000494058.6:n.3759G=
ENST00000697831.1:c.3388G=	ENSP00000513453.1:p.Gly1130=
ENST00000697832.1:n.3610G=
ENST00000697833.1:c.*405G=	ENSP00000513454.1:n.*405G=
ENST00000697834.1:n.4081G=
ENST00000697835.1:c.*2975G=	ENSP00000513455.1:n.*2975G=
ENST00000697836.1:n.3788G=
ENST00000697837.1:c.*573G=	ENSP00000513456.1:n.*573G=
ENST00000697838.1:c.3322G=	ENSP00000513457.1:p.Gly1108=
ENST00000697839.1:n.4175G=
ENST00000697840.1:c.3493G=	ENSP00000513458.1:p.Gly1165=
ENST00000697841.1:n.4274G=
ENST00000697842.1:n.3712G=
ENST00000375394.7:c.3457G= MANE Select	ENSP00000364543.2:p.Gly1153=
ENST00000375394.6:c.3457G=	ENSP00000364543.2:p.Gly1153=
ENST00000465703.5:n.4093G=
ENST00000470453.1:n.382+21G=
ENST00000471818.1:n.386G=
ENST00000474839.5:c.*2829G=	ENSP00000420470.1:n.*2829G=
ENST00000483553.5:c.893G=
ENST00000485349.5:n.663G=
ENST00000491994.1:c.452G=
NM_006929.4:c.3457G=	NP_008860.4:p.Gly1153=
XR_001743586.2:n.3556G=
XR_926301.3:n.3473G=
NM_006929.5:c.3457G= MANE Select	NP_008860.4:p.Gly1153=