Canonical Allele Identifier: CA1619384327

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969378T= , CM000668.2:g.31969378T=	GRCh38
NC_000006.11:g.31937155T= , CM000668.1:g.31937155T=	GRCh37
NC_000006.10:g.32045134T=	NCBI36
NG_032652.1:g.15575T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2452T=	ENSP00000419905.1:n.*2452T=
ENST00000483553.6:c.*465T=	ENSP00000420332.2:n.*465T=
ENST00000485349.6:n.3974T=
ENST00000491994.2:c.3498T=	ENSP00000417586.2:p.Asn1166=
ENST00000494058.6:n.3800T=
ENST00000697831.1:c.3429T=	ENSP00000513453.1:p.Asn1143=
ENST00000697832.1:n.3651T=
ENST00000697833.1:c.*446T=	ENSP00000513454.1:n.*446T=
ENST00000697834.1:n.4122T=
ENST00000697835.1:c.*3016T=	ENSP00000513455.1:n.*3016T=
ENST00000697836.1:n.3829T=
ENST00000697837.1:c.*614T=	ENSP00000513456.1:n.*614T=
ENST00000697838.1:c.3363T=	ENSP00000513457.1:p.Asn1121=
ENST00000697839.1:n.4216T=
ENST00000697840.1:c.3534T=	ENSP00000513458.1:p.Asn1178=
ENST00000697841.1:n.4315T=
ENST00000697842.1:n.3753T=
ENST00000375394.7:c.3498T= MANE Select	ENSP00000364543.2:p.Asn1166=
ENST00000375394.6:c.3498T=	ENSP00000364543.2:p.Asn1166=
ENST00000465703.5:n.4134T=
ENST00000470453.1:n.382+62T=
ENST00000471818.1:n.427T=
ENST00000474839.5:c.*2870T=	ENSP00000420470.1:n.*2870T=
ENST00000483553.5:c.934T=
ENST00000485349.5:n.704T=
ENST00000491994.1:c.493T=
NM_006929.4:c.3498T=	NP_008860.4:p.Asn1166=
XR_001743586.2:n.3597T=
XR_926301.3:n.3514T=
NM_006929.5:c.3498T= MANE Select	NP_008860.4:p.Asn1166=