Canonical Allele Identifier: CA2830539175

Gene: SKIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516759A>C , CM000667.2:g.95516759A>C	GRCh38
NC_000005.9:g.94852463A>C , CM000667.1:g.94852463A>C	GRCh37
NC_000005.8:g.94878219A>C	NCBI36
NG_023414.1:g.43247T>G , LRG_173:g.43247T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506007.2:n.2883T>G
ENST00000513232.2:c.*1308T>G	ENSP00000422749.2:n.*1308T>G
ENST00000698450.1:n.1821-9T>G
ENST00000698451.1:n.2013T>G
ENST00000698452.1:n.3084T>G
ENST00000698453.1:c.2441+152T>G	ENSP00000513735.1:n.2441+152T>G
ENST00000698454.1:c.2428-9T>G	ENSP00000513736.1:n.2428-9T>G
ENST00000698455.1:c.*2569T>G	ENSP00000513737.1:n.*2569T>G
ENST00000698456.1:c.*1295-9T>G	ENSP00000513738.1:n.*1295-9T>G
ENST00000698457.1:c.2227-9T>G	ENSP00000513739.1:n.2227-9T>G
ENST00000698458.1:c.2477+152T>G	ENSP00000513740.1:n.2477+152T>G
ENST00000698459.1:c.2437-9T>G	ENSP00000513741.1:n.2437-9T>G
ENST00000698460.1:c.*278+157T>G	ENSP00000513742.1:n.*278+157T>G
ENST00000698461.1:n.2883T>G
ENST00000698462.1:n.2812-9T>G
ENST00000698468.1:n.3084T>G
ENST00000698469.1:c.*1940T>G	ENSP00000513743.1:n.*1940T>G
ENST00000698470.1:c.*435T>G	ENSP00000513744.1:n.*435T>G
ENST00000698471.1:n.2883T>G
ENST00000698472.1:c.*1308T>G	ENSP00000513745.1:n.*1308T>G
ENST00000698473.1:n.2883T>G
ENST00000698474.1:n.2883T>G
ENST00000698475.1:n.2968T>G
ENST00000698476.1:c.2437-9T>G	ENSP00000513746.1:n.2437-9T>G
ENST00000698477.1:c.2441+152T>G	ENSP00000513747.1:n.2441+152T>G
ENST00000698478.1:n.2883T>G
ENST00000698479.1:c.2437-9T>G	ENSP00000513748.1:n.2437-9T>G
ENST00000698480.1:c.2436+157T>G	ENSP00000513749.1:n.2436+157T>G
ENST00000698481.1:c.2436+157T>G	ENSP00000513750.1:n.2436+157T>G
ENST00000698482.1:n.2727-9T>G
ENST00000698483.1:n.2883T>G
ENST00000698484.1:c.2437-9T>G	ENSP00000513751.1:n.2437-9T>G
ENST00000698485.1:c.2436+157T>G	ENSP00000513752.1:n.2436+157T>G
ENST00000698486.1:n.2883T>G
ENST00000698487.1:c.2437-9T>G	ENSP00000513753.1:n.2437-9T>G
ENST00000698488.1:c.2259+157T>G	ENSP00000513754.1:n.2259+157T>G
ENST00000698489.1:n.6668T>G
ENST00000698490.1:c.2437-9T>G	ENSP00000513755.1:n.2437-9T>G
ENST00000698492.1:c.*1152-9T>G	ENSP00000513756.1:n.*1152-9T>G
ENST00000698493.1:n.2727-9T>G
ENST00000698494.1:c.*323T>G	ENSP00000513757.1:n.*323T>G
ENST00000358746.7:c.2437-9T>G MANE Select	ENSP00000351596.3:n.2437-9T>G
ENST00000649566.1:c.2437-9T>G	ENSP00000497948.1:n.2437-9T>G
ENST00000358746.6:c.2437-9T>G	ENSP00000351596.2:n.2437-9T>G
ENST00000506007.1:n.10T>G
ENST00000507805.5:n.615T>G
NM_014639.3:c.2437-9T>G , LRG_173t1:c.2437-9T>G	NP_055454.1:n.2437-9T>G
XR_948312.1:n.2706-9T>G
XR_001742370.2:n.2709-9T>G
NM_014639.4:c.2437-9T>G MANE Select	NP_055454.1:n.2437-9T>G