Canonical Allele Identifier: CA1619384461

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969706C= , CM000668.2:g.31969706C=	GRCh38
NC_000006.11:g.31937483C= , CM000668.1:g.31937483C=	GRCh37
NC_000006.10:g.32045462C=	NCBI36
NG_032652.1:g.15903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2780C=	ENSP00000419905.1:n.*2780C=
ENST00000485349.6:n.4208C=
ENST00000491994.2:c.*274C=	ENSP00000417586.2:n.*274C=
ENST00000494058.6:n.4034C=
ENST00000697831.1:c.3663C=	ENSP00000513453.1:p.Tyr1221=
ENST00000697832.1:n.3885C=
ENST00000697834.1:n.4450C=
ENST00000697835.1:c.*3250C=	ENSP00000513455.1:n.*3250C=
ENST00000697837.1:c.*848C=	ENSP00000513456.1:n.*848C=
ENST00000697838.1:c.3597C=	ENSP00000513457.1:p.Tyr1199=
ENST00000697839.1:n.4544C=
ENST00000697840.1:c.3768C=	ENSP00000513458.1:p.Tyr1256=
ENST00000697841.1:n.4643C=
ENST00000697842.1:n.3987C=
ENST00000375394.7:c.3732C= MANE Select	ENSP00000364543.2:p.Tyr1244=
ENST00000375394.6:c.3732C=	ENSP00000364543.2:p.Tyr1244=
ENST00000465703.5:n.4462C=
ENST00000471818.1:n.661C=
ENST00000474839.5:c.*3104C=	ENSP00000420470.1:n.*3104C=
ENST00000483553.5:c.1262C=
ENST00000491994.1:c.821C=
NM_006929.4:c.3732C=	NP_008860.4:p.Tyr1244=
XR_926301.3:n.3748C=
NM_006929.5:c.3732C= MANE Select	NP_008860.4:p.Tyr1244=