Canonical Allele Identifier: CA1619384334

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969400T= , CM000668.2:g.31969400T=	GRCh38
NC_000006.11:g.31937177T= , CM000668.1:g.31937177T=	GRCh37
NC_000006.10:g.32045156T=	NCBI36
NG_032652.1:g.15597T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2474T=	ENSP00000419905.1:n.*2474T=
ENST00000483553.6:c.*487T=	ENSP00000420332.2:n.*487T=
ENST00000485349.6:n.3996T=
ENST00000491994.2:c.3520T=	ENSP00000417586.2:p.Tyr1174=
ENST00000494058.6:n.3822T=
ENST00000697831.1:c.3451T=	ENSP00000513453.1:p.Tyr1151=
ENST00000697832.1:n.3673T=
ENST00000697833.1:c.*468T=	ENSP00000513454.1:n.*468T=
ENST00000697834.1:n.4144T=
ENST00000697835.1:c.*3038T=	ENSP00000513455.1:n.*3038T=
ENST00000697836.1:n.3851T=
ENST00000697837.1:c.*636T=	ENSP00000513456.1:n.*636T=
ENST00000697838.1:c.3385T=	ENSP00000513457.1:p.Tyr1129=
ENST00000697839.1:n.4238T=
ENST00000697840.1:c.3556T=	ENSP00000513458.1:p.Tyr1186=
ENST00000697841.1:n.4337T=
ENST00000697842.1:n.3775T=
ENST00000375394.7:c.3520T= MANE Select	ENSP00000364543.2:p.Tyr1174=
ENST00000375394.6:c.3520T=	ENSP00000364543.2:p.Tyr1174=
ENST00000465703.5:n.4156T=
ENST00000470453.1:n.382+84T=
ENST00000471818.1:n.449T=
ENST00000474839.5:c.*2892T=	ENSP00000420470.1:n.*2892T=
ENST00000483553.5:c.956T=
ENST00000485349.5:n.726T=
ENST00000491994.1:c.515T=
NM_006929.4:c.3520T=	NP_008860.4:p.Tyr1174=
XR_001743586.2:n.3619T=
XR_926301.3:n.3536T=
NM_006929.5:c.3520T= MANE Select	NP_008860.4:p.Tyr1174=