Canonical Allele Identifier: CA363490299

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937180G>C (hg19) ; chr6:g.31969403G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969403G>C , CM000668.2:g.31969403G>C	GRCh38
NC_000006.11:g.31937180G>C , CM000668.1:g.31937180G>C	GRCh37
NC_000006.10:g.32045159G>C	NCBI36
NG_032652.1:g.15600G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2477G>C	ENSP00000419905.1:n.*2477G>C
ENST00000483553.6:c.*490G>C	ENSP00000420332.2:n.*490G>C
ENST00000485349.6:n.3999G>C
ENST00000491994.2:c.3523G>C	ENSP00000417586.2:p.Glu1175Gln
ENST00000494058.6:n.3825G>C
ENST00000697831.1:c.3454G>C	ENSP00000513453.1:p.Glu1152Gln
ENST00000697832.1:n.3676G>C
ENST00000697833.1:c.*471G>C	ENSP00000513454.1:n.*471G>C
ENST00000697834.1:n.4147G>C
ENST00000697835.1:c.*3041G>C	ENSP00000513455.1:n.*3041G>C
ENST00000697836.1:n.3854G>C
ENST00000697837.1:c.*639G>C	ENSP00000513456.1:n.*639G>C
ENST00000697838.1:c.3388G>C	ENSP00000513457.1:p.Glu1130Gln
ENST00000697839.1:n.4241G>C
ENST00000697840.1:c.3559G>C	ENSP00000513458.1:p.Glu1187Gln
ENST00000697841.1:n.4340G>C
ENST00000697842.1:n.3778G>C
ENST00000375394.7:c.3523G>C MANE Select	ENSP00000364543.2:p.Glu1175Gln
ENST00000375394.6:c.3523G>C	ENSP00000364543.2:p.Glu1175Gln
ENST00000465703.5:n.4159G>C
ENST00000470453.1:n.382+87G>C
ENST00000471818.1:n.452G>C
ENST00000474839.5:c.*2895G>C	ENSP00000420470.1:n.*2895G>C
ENST00000483553.5:c.959G>C
ENST00000485349.5:n.729G>C
ENST00000491994.1:c.518G>C
NM_006929.4:c.3523G>C	NP_008860.4:p.Glu1175Gln
XR_001743586.2:n.3622G>C
XR_926301.3:n.3539G>C
NM_006929.5:c.3523G>C MANE Select	NP_008860.4:p.Glu1175Gln