Canonical Allele Identifier: CA1619384433

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969640G= , CM000668.2:g.31969640G=	GRCh38
NC_000006.11:g.31937417G= , CM000668.1:g.31937417G=	GRCh37
NC_000006.10:g.32045396G=	NCBI36
NG_032652.1:g.15837G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2714G=	ENSP00000419905.1:n.*2714G=
ENST00000485349.6:n.4142G=
ENST00000491994.2:c.*208G=	ENSP00000417586.2:n.*208G=
ENST00000494058.6:n.3968G=
ENST00000697831.1:c.3597G=	ENSP00000513453.1:p.Leu1199=
ENST00000697832.1:n.3819G=
ENST00000697834.1:n.4384G=
ENST00000697835.1:c.*3184G=	ENSP00000513455.1:n.*3184G=
ENST00000697836.1:n.4020G=
ENST00000697837.1:c.*782G=	ENSP00000513456.1:n.*782G=
ENST00000697838.1:c.3531G=	ENSP00000513457.1:p.Leu1177=
ENST00000697839.1:n.4478G=
ENST00000697840.1:c.3702G=	ENSP00000513458.1:p.Leu1234=
ENST00000697841.1:n.4577G=
ENST00000697842.1:n.3921G=
ENST00000375394.7:c.3666G= MANE Select	ENSP00000364543.2:p.Leu1222=
ENST00000375394.6:c.3666G=	ENSP00000364543.2:p.Leu1222=
ENST00000465703.5:n.4396G=
ENST00000471818.1:n.595G=
ENST00000474839.5:c.*3038G=	ENSP00000420470.1:n.*3038G=
ENST00000483553.5:c.1196G=
ENST00000491994.1:c.755G=
NM_006929.4:c.3666G=	NP_008860.4:p.Leu1222=
XR_926301.3:n.3682G=
NM_006929.5:c.3666G= MANE Select	NP_008860.4:p.Leu1222=