Canonical Allele Identifier: CA360457853

Gene: SKIC3

Linked Data

• MyVariant Identifiers: chr5:g.94852277A>C (hg19) ; chr5:g.95516573A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516573A>C , CM000667.2:g.95516573A>C	GRCh38
NC_000005.9:g.94852277A>C , CM000667.1:g.94852277A>C	GRCh37
NC_000005.8:g.94878033A>C	NCBI36
NG_023414.1:g.43433T>G , LRG_173:g.43433T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000506007.2:n.3069T>G
ENST00000513232.2:c.*1494T>G	ENSP00000422749.2:n.*1494T>G
ENST00000698450.1:n.1913T>G
ENST00000698451.1:n.2199T>G
ENST00000698452.1:n.3270T>G
ENST00000698453.1:c.2455T>G	ENSP00000513735.1:p.Cys819Gly
ENST00000698454.1:c.2520T>G	ENSP00000513736.1:p.Tyr840Ter
ENST00000698455.1:c.*2755T>G	ENSP00000513737.1:n.*2755T>G
ENST00000698456.1:c.*1387T>G	ENSP00000513738.1:n.*1387T>G
ENST00000698457.1:c.2319T>G	ENSP00000513739.1:p.Tyr773Ter
ENST00000698458.1:c.2491T>G	ENSP00000513740.1:p.Cys831Gly
ENST00000698459.1:c.2529T>G	ENSP00000513741.1:p.Tyr843Ter
ENST00000698460.1:c.*292T>G	ENSP00000513742.1:n.*292T>G
ENST00000698461.1:n.2984T>G
ENST00000698462.1:n.2904T>G
ENST00000698468.1:n.3270T>G
ENST00000698469.1:c.*2126T>G	ENSP00000513743.1:n.*2126T>G
ENST00000698470.1:c.*621T>G	ENSP00000513744.1:n.*621T>G
ENST00000698471.1:n.3069T>G
ENST00000698472.1:c.*1494T>G	ENSP00000513745.1:n.*1494T>G
ENST00000698473.1:n.3069T>G
ENST00000698474.1:n.3069T>G
ENST00000698475.1:n.3154T>G
ENST00000698476.1:c.2529T>G	ENSP00000513746.1:p.Tyr843Ter
ENST00000698477.1:c.2455T>G	ENSP00000513747.1:p.Cys819Gly
ENST00000698478.1:n.3069T>G
ENST00000698479.1:c.2529T>G	ENSP00000513748.1:p.Tyr843Ter
ENST00000698480.1:c.2450T>G	ENSP00000513749.1:p.Met817Arg
ENST00000698481.1:c.2450T>G	ENSP00000513750.1:p.Met817Arg
ENST00000698482.1:n.2819T>G
ENST00000698483.1:n.2984T>G
ENST00000698484.1:c.2529T>G	ENSP00000513751.1:p.Tyr843Ter
ENST00000698485.1:c.2450T>G	ENSP00000513752.1:p.Met817Arg
ENST00000698486.1:n.3069T>G
ENST00000698487.1:c.2529T>G	ENSP00000513753.1:p.Tyr843Ter
ENST00000698488.1:c.2273T>G	ENSP00000513754.1:p.Met758Arg
ENST00000698489.1:n.6854T>G
ENST00000698490.1:c.2529T>G	ENSP00000513755.1:p.Tyr843Ter
ENST00000698492.1:c.*1244T>G	ENSP00000513756.1:n.*1244T>G
ENST00000698493.1:n.2819T>G
ENST00000698494.1:c.*509T>G	ENSP00000513757.1:n.*509T>G
ENST00000358746.7:c.2529T>G MANE Select	ENSP00000351596.3:p.Tyr843Ter
ENST00000649566.1:c.2529T>G	ENSP00000497948.1:p.Tyr843Ter
ENST00000358746.6:c.2529T>G	ENSP00000351596.2:p.Tyr843Ter
ENST00000506007.1:n.196T>G
ENST00000507805.5:n.801T>G
ENST00000508181.5:n.102T>G
NM_014639.3:c.2529T>G , LRG_173t1:c.2529T>G	NP_055454.1:p.Tyr843Ter
XR_948312.1:n.2798T>G
XR_001742370.2:n.2801T>G
NM_014639.4:c.2529T>G MANE Select	NP_055454.1:p.Tyr843Ter