Canonical Allele Identifier: CA449814110

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937345C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969568C>A , CM000668.2:g.31969568C>A	GRCh38
NC_000006.11:g.31937345C>A , CM000668.1:g.31937345C>A	GRCh37
NC_000006.10:g.32045324C>A	NCBI36
NG_032652.1:g.15765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2642C>A	ENSP00000419905.1:n.*2642C>A
ENST00000485349.6:n.4070C>A
ENST00000491994.2:c.*136C>A	ENSP00000417586.2:n.*136C>A
ENST00000494058.6:n.3896C>A
ENST00000697831.1:c.3525C>A	ENSP00000513453.1:p.Arg1175=
ENST00000697832.1:n.3747C>A
ENST00000697833.1:c.*542C>A	ENSP00000513454.1:n.*542C>A
ENST00000697834.1:n.4312C>A
ENST00000697835.1:c.*3112C>A	ENSP00000513455.1:n.*3112C>A
ENST00000697836.1:n.3948C>A
ENST00000697837.1:c.*710C>A	ENSP00000513456.1:n.*710C>A
ENST00000697838.1:c.3459C>A	ENSP00000513457.1:p.Arg1153=
ENST00000697839.1:n.4406C>A
ENST00000697840.1:c.3630C>A	ENSP00000513458.1:p.Arg1210=
ENST00000697841.1:n.4505C>A
ENST00000697842.1:n.3849C>A
ENST00000375394.7:c.3594C>A MANE Select	ENSP00000364543.2:p.Arg1198=
ENST00000375394.6:c.3594C>A	ENSP00000364543.2:p.Arg1198=
ENST00000465703.5:n.4324C>A
ENST00000470453.1:n.436C>A
ENST00000471818.1:n.523C>A
ENST00000474839.5:c.*2966C>A	ENSP00000420470.1:n.*2966C>A
ENST00000483553.5:c.1124C>A
ENST00000491994.1:c.683C>A
NM_006929.4:c.3594C>A	NP_008860.4:p.Arg1198=
XR_926301.3:n.3610C>A
NM_006929.5:c.3594C>A MANE Select	NP_008860.4:p.Arg1198=