Canonical Allele Identifier: CA1619384409

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969597G= , CM000668.2:g.31969597G=	GRCh38
NC_000006.11:g.31937374G= , CM000668.1:g.31937374G=	GRCh37
NC_000006.10:g.32045353G=	NCBI36
NG_032652.1:g.15794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2671G=	ENSP00000419905.1:n.*2671G=
ENST00000485349.6:n.4099G=
ENST00000491994.2:c.*165G=	ENSP00000417586.2:n.*165G=
ENST00000494058.6:n.3925G=
ENST00000697831.1:c.3554G=	ENSP00000513453.1:p.Arg1185=
ENST00000697832.1:n.3776G=
ENST00000697834.1:n.4341G=
ENST00000697835.1:c.*3141G=	ENSP00000513455.1:n.*3141G=
ENST00000697836.1:n.3977G=
ENST00000697837.1:c.*739G=	ENSP00000513456.1:n.*739G=
ENST00000697838.1:c.3488G=	ENSP00000513457.1:p.Arg1163=
ENST00000697839.1:n.4435G=
ENST00000697840.1:c.3659G=	ENSP00000513458.1:p.Arg1220=
ENST00000697841.1:n.4534G=
ENST00000697842.1:n.3878G=
ENST00000375394.7:c.3623G= MANE Select	ENSP00000364543.2:p.Arg1208=
ENST00000375394.6:c.3623G=	ENSP00000364543.2:p.Arg1208=
ENST00000465703.5:n.4353G=
ENST00000471818.1:n.552G=
ENST00000474839.5:c.*2995G=	ENSP00000420470.1:n.*2995G=
ENST00000483553.5:c.1153G=
ENST00000491994.1:c.712G=
NM_006929.4:c.3623G=	NP_008860.4:p.Arg1208=
XR_926301.3:n.3639G=
NM_006929.5:c.3623G= MANE Select	NP_008860.4:p.Arg1208=