Canonical Allele Identifier: CA363450459

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31930248G>C (hg19) ; chr6:g.31962471G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31962471G>C , CM000668.2:g.31962471G>C	GRCh38
NC_000006.11:g.31930248G>C , CM000668.1:g.31930248G>C	GRCh37
NC_000006.10:g.32038227G>C	NCBI36
NG_032652.1:g.8668G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*213G>C	ENSP00000419905.1:n.*213G>C
ENST00000483553.6:c.1097G>C	ENSP00000420332.2:p.Ser366Thr
ENST00000485349.6:n.1138G>C
ENST00000491994.2:c.1097G>C	ENSP00000417586.2:p.Ser366Thr
ENST00000494058.6:n.1154G>C
ENST00000697831.1:c.1097G>C	ENSP00000513453.1:p.Ser366Thr
ENST00000697832.1:n.1173G>C
ENST00000697833.1:c.1097G>C	ENSP00000513454.1:p.Ser366Thr
ENST00000697834.1:n.1149G>C
ENST00000697835.1:c.*615G>C	ENSP00000513455.1:n.*615G>C
ENST00000697836.1:n.1133G>C
ENST00000697837.1:c.1097G>C	ENSP00000513456.1:p.Ser366Thr
ENST00000697838.1:c.962G>C	ENSP00000513457.1:p.Ser321Thr
ENST00000697839.1:n.1380G>C
ENST00000697840.1:c.1133G>C	ENSP00000513458.1:p.Ser378Thr
ENST00000697841.1:n.1669G>C
ENST00000697842.1:n.1097G>C
ENST00000375394.7:c.1097G>C MANE Select	ENSP00000364543.2:p.Ser366Thr
ENST00000375394.6:c.1097G>C	ENSP00000364543.2:p.Ser366Thr
ENST00000461073.5:c.*213G>C	ENSP00000419905.1:n.*213G>C
ENST00000465703.5:n.1410G>C
ENST00000466290.1:n.358G>C
ENST00000474839.5:c.*469G>C	ENSP00000420470.1:n.*469G>C
NM_006929.4:c.1097G>C	NP_008860.4:p.Ser366Thr
XM_006715168.2:c.1097G>C	XP_006715231.1:p.Ser366Thr
XM_011514815.1:c.1097G>C	XP_011513117.1:p.Ser366Thr
XR_926301.1:n.1185G>C
XM_011514815.3:c.1097G>C	XP_011513117.1:p.Ser366Thr
XR_001743586.2:n.1133G>C
XR_926301.3:n.1133G>C
NM_006929.5:c.1097G>C MANE Select	NP_008860.4:p.Ser366Thr