Canonical Allele Identifier: CA1619384335

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969402T= , CM000668.2:g.31969402T=	GRCh38
NC_000006.11:g.31937179T= , CM000668.1:g.31937179T=	GRCh37
NC_000006.10:g.32045158T=	NCBI36
NG_032652.1:g.15599T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2476T=	ENSP00000419905.1:n.*2476T=
ENST00000483553.6:c.*489T=	ENSP00000420332.2:n.*489T=
ENST00000485349.6:n.3998T=
ENST00000491994.2:c.3522T=	ENSP00000417586.2:p.Tyr1174=
ENST00000494058.6:n.3824T=
ENST00000697831.1:c.3453T=	ENSP00000513453.1:p.Tyr1151=
ENST00000697832.1:n.3675T=
ENST00000697833.1:c.*470T=	ENSP00000513454.1:n.*470T=
ENST00000697834.1:n.4146T=
ENST00000697835.1:c.*3040T=	ENSP00000513455.1:n.*3040T=
ENST00000697836.1:n.3853T=
ENST00000697837.1:c.*638T=	ENSP00000513456.1:n.*638T=
ENST00000697838.1:c.3387T=	ENSP00000513457.1:p.Tyr1129=
ENST00000697839.1:n.4240T=
ENST00000697840.1:c.3558T=	ENSP00000513458.1:p.Tyr1186=
ENST00000697841.1:n.4339T=
ENST00000697842.1:n.3777T=
ENST00000375394.7:c.3522T= MANE Select	ENSP00000364543.2:p.Tyr1174=
ENST00000375394.6:c.3522T=	ENSP00000364543.2:p.Tyr1174=
ENST00000465703.5:n.4158T=
ENST00000470453.1:n.382+86T=
ENST00000471818.1:n.451T=
ENST00000474839.5:c.*2894T=	ENSP00000420470.1:n.*2894T=
ENST00000483553.5:c.958T=
ENST00000485349.5:n.728T=
ENST00000491994.1:c.517T=
NM_006929.4:c.3522T=	NP_008860.4:p.Tyr1174=
XR_001743586.2:n.3621T=
XR_926301.3:n.3538T=
NM_006929.5:c.3522T= MANE Select	NP_008860.4:p.Tyr1174=