Canonical Allele Identifier: CA449814143

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937375C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969598C>A , CM000668.2:g.31969598C>A	GRCh38
NC_000006.11:g.31937375C>A , CM000668.1:g.31937375C>A	GRCh37
NC_000006.10:g.32045354C>A	NCBI36
NG_032652.1:g.15795C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2672C>A	ENSP00000419905.1:n.*2672C>A
ENST00000485349.6:n.4100C>A
ENST00000491994.2:c.*166C>A	ENSP00000417586.2:n.*166C>A
ENST00000494058.6:n.3926C>A
ENST00000697831.1:c.3555C>A	ENSP00000513453.1:p.Arg1185=
ENST00000697832.1:n.3777C>A
ENST00000697834.1:n.4342C>A
ENST00000697835.1:c.*3142C>A	ENSP00000513455.1:n.*3142C>A
ENST00000697836.1:n.3978C>A
ENST00000697837.1:c.*740C>A	ENSP00000513456.1:n.*740C>A
ENST00000697838.1:c.3489C>A	ENSP00000513457.1:p.Arg1163=
ENST00000697839.1:n.4436C>A
ENST00000697840.1:c.3660C>A	ENSP00000513458.1:p.Arg1220=
ENST00000697841.1:n.4535C>A
ENST00000697842.1:n.3879C>A
ENST00000375394.7:c.3624C>A MANE Select	ENSP00000364543.2:p.Arg1208=
ENST00000375394.6:c.3624C>A	ENSP00000364543.2:p.Arg1208=
ENST00000465703.5:n.4354C>A
ENST00000471818.1:n.553C>A
ENST00000474839.5:c.*2996C>A	ENSP00000420470.1:n.*2996C>A
ENST00000483553.5:c.1154C>A
ENST00000491994.1:c.713C>A
NM_006929.4:c.3624C>A	NP_008860.4:p.Arg1208=
XR_926301.3:n.3640C>A
NM_006929.5:c.3624C>A MANE Select	NP_008860.4:p.Arg1208=