Canonical Allele Identifier: CA1619384305

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969335G= , CM000668.2:g.31969335G=	GRCh38
NC_000006.11:g.31937112G= , CM000668.1:g.31937112G=	GRCh37
NC_000006.10:g.32045091G=	NCBI36
NG_032652.1:g.15532G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2409G=	ENSP00000419905.1:n.*2409G=
ENST00000483553.6:c.*422G=	ENSP00000420332.2:n.*422G=
ENST00000485349.6:n.3931G=
ENST00000491994.2:c.3455G=	ENSP00000417586.2:p.Cys1152=
ENST00000494058.6:n.3757G=
ENST00000697831.1:c.3386G=	ENSP00000513453.1:p.Cys1129=
ENST00000697832.1:n.3608G=
ENST00000697833.1:c.*403G=	ENSP00000513454.1:n.*403G=
ENST00000697834.1:n.4079G=
ENST00000697835.1:c.*2973G=	ENSP00000513455.1:n.*2973G=
ENST00000697836.1:n.3786G=
ENST00000697837.1:c.*571G=	ENSP00000513456.1:n.*571G=
ENST00000697838.1:c.3320G=	ENSP00000513457.1:p.Cys1107=
ENST00000697839.1:n.4173G=
ENST00000697840.1:c.3491G=	ENSP00000513458.1:p.Cys1164=
ENST00000697841.1:n.4272G=
ENST00000697842.1:n.3710G=
ENST00000375394.7:c.3455G= MANE Select	ENSP00000364543.2:p.Cys1152=
ENST00000375394.6:c.3455G=	ENSP00000364543.2:p.Cys1152=
ENST00000465703.5:n.4091G=
ENST00000470453.1:n.382+19G=
ENST00000471818.1:n.384G=
ENST00000474839.5:c.*2827G=	ENSP00000420470.1:n.*2827G=
ENST00000483553.5:c.891G=
ENST00000485349.5:n.661G=
ENST00000491994.1:c.450G=
NM_006929.4:c.3455G=	NP_008860.4:p.Cys1152=
XR_001743586.2:n.3554G=
XR_926301.3:n.3471G=
NM_006929.5:c.3455G= MANE Select	NP_008860.4:p.Cys1152=