Canonical Allele Identifier: CA649725437

Gene: SKIC3

Linked Data

• COSMIC: COSN8790574

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516761G>A , CM000667.2:g.95516761G>A	GRCh38
NC_000005.9:g.94852465G>A , CM000667.1:g.94852465G>A	GRCh37
NC_000005.8:g.94878221G>A	NCBI36
NG_023414.1:g.43245C>T , LRG_173:g.43245C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506007.2:n.2881C>T
ENST00000513232.2:c.*1306C>T	ENSP00000422749.2:n.*1306C>T
ENST00000698450.1:n.1821-11C>T
ENST00000698451.1:n.2011C>T
ENST00000698452.1:n.3082C>T
ENST00000698453.1:c.2441+150C>T	ENSP00000513735.1:n.2441+150C>T
ENST00000698454.1:c.2428-11C>T	ENSP00000513736.1:n.2428-11C>T
ENST00000698455.1:c.*2567C>T	ENSP00000513737.1:n.*2567C>T
ENST00000698456.1:c.*1295-11C>T	ENSP00000513738.1:n.*1295-11C>T
ENST00000698457.1:c.2227-11C>T	ENSP00000513739.1:n.2227-11C>T
ENST00000698458.1:c.2477+150C>T	ENSP00000513740.1:n.2477+150C>T
ENST00000698459.1:c.2437-11C>T	ENSP00000513741.1:n.2437-11C>T
ENST00000698460.1:c.*278+155C>T	ENSP00000513742.1:n.*278+155C>T
ENST00000698461.1:n.2881C>T
ENST00000698462.1:n.2812-11C>T
ENST00000698468.1:n.3082C>T
ENST00000698469.1:c.*1938C>T	ENSP00000513743.1:n.*1938C>T
ENST00000698470.1:c.*433C>T	ENSP00000513744.1:n.*433C>T
ENST00000698471.1:n.2881C>T
ENST00000698472.1:c.*1306C>T	ENSP00000513745.1:n.*1306C>T
ENST00000698473.1:n.2881C>T
ENST00000698474.1:n.2881C>T
ENST00000698475.1:n.2966C>T
ENST00000698476.1:c.2437-11C>T	ENSP00000513746.1:n.2437-11C>T
ENST00000698477.1:c.2441+150C>T	ENSP00000513747.1:n.2441+150C>T
ENST00000698478.1:n.2881C>T
ENST00000698479.1:c.2437-11C>T	ENSP00000513748.1:n.2437-11C>T
ENST00000698480.1:c.2436+155C>T	ENSP00000513749.1:n.2436+155C>T
ENST00000698481.1:c.2436+155C>T	ENSP00000513750.1:n.2436+155C>T
ENST00000698482.1:n.2727-11C>T
ENST00000698483.1:n.2881C>T
ENST00000698484.1:c.2437-11C>T	ENSP00000513751.1:n.2437-11C>T
ENST00000698485.1:c.2436+155C>T	ENSP00000513752.1:n.2436+155C>T
ENST00000698486.1:n.2881C>T
ENST00000698487.1:c.2437-11C>T	ENSP00000513753.1:n.2437-11C>T
ENST00000698488.1:c.2259+155C>T	ENSP00000513754.1:n.2259+155C>T
ENST00000698489.1:n.6666C>T
ENST00000698490.1:c.2437-11C>T	ENSP00000513755.1:n.2437-11C>T
ENST00000698492.1:c.*1152-11C>T	ENSP00000513756.1:n.*1152-11C>T
ENST00000698493.1:n.2727-11C>T
ENST00000698494.1:c.*321C>T	ENSP00000513757.1:n.*321C>T
ENST00000358746.7:c.2437-11C>T MANE Select	ENSP00000351596.3:n.2437-11C>T
ENST00000649566.1:c.2437-11C>T	ENSP00000497948.1:n.2437-11C>T
ENST00000358746.6:c.2437-11C>T	ENSP00000351596.2:n.2437-11C>T
ENST00000506007.1:n.8C>T
ENST00000507805.5:n.613C>T
NM_014639.3:c.2437-11C>T , LRG_173t1:c.2437-11C>T	NP_055454.1:n.2437-11C>T
XR_948312.1:n.2706-11C>T
XR_001742370.2:n.2709-11C>T
NM_014639.4:c.2437-11C>T MANE Select	NP_055454.1:n.2437-11C>T