Canonical Allele Identifier: CA360457869

Gene: SKIC3

Linked Data

• gnomAD v4: 5-95516576-A-C
• MyVariant Identifiers: chr5:g.94852280A>C (hg19) ; chr5:g.95516576A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516576A>C , CM000667.2:g.95516576A>C	GRCh38
NC_000005.9:g.94852280A>C , CM000667.1:g.94852280A>C	GRCh37
NC_000005.8:g.94878036A>C	NCBI36
NG_023414.1:g.43430T>G , LRG_173:g.43430T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000506007.2:n.3066T>G
ENST00000513232.2:c.*1491T>G	ENSP00000422749.2:n.*1491T>G
ENST00000698450.1:n.1910T>G
ENST00000698451.1:n.2196T>G
ENST00000698452.1:n.3267T>G
ENST00000698453.1:c.2452T>G	ENSP00000513735.1:p.Leu818Val
ENST00000698454.1:c.2517T>G	ENSP00000513736.1:p.Asn839Lys
ENST00000698455.1:c.*2752T>G	ENSP00000513737.1:n.*2752T>G
ENST00000698456.1:c.*1384T>G	ENSP00000513738.1:n.*1384T>G
ENST00000698457.1:c.2316T>G	ENSP00000513739.1:p.Asn772Lys
ENST00000698458.1:c.2488T>G	ENSP00000513740.1:p.Leu830Val
ENST00000698459.1:c.2526T>G	ENSP00000513741.1:p.Asn842Lys
ENST00000698460.1:c.*289T>G	ENSP00000513742.1:n.*289T>G
ENST00000698461.1:n.2981T>G
ENST00000698462.1:n.2901T>G
ENST00000698468.1:n.3267T>G
ENST00000698469.1:c.*2123T>G	ENSP00000513743.1:n.*2123T>G
ENST00000698470.1:c.*618T>G	ENSP00000513744.1:n.*618T>G
ENST00000698471.1:n.3066T>G
ENST00000698472.1:c.*1491T>G	ENSP00000513745.1:n.*1491T>G
ENST00000698473.1:n.3066T>G
ENST00000698474.1:n.3066T>G
ENST00000698475.1:n.3151T>G
ENST00000698476.1:c.2526T>G	ENSP00000513746.1:p.Asn842Lys
ENST00000698477.1:c.2452T>G	ENSP00000513747.1:p.Leu818Val
ENST00000698478.1:n.3066T>G
ENST00000698479.1:c.2526T>G	ENSP00000513748.1:p.Asn842Lys
ENST00000698480.1:c.2447T>G	ENSP00000513749.1:p.Ile816Ser
ENST00000698481.1:c.2447T>G	ENSP00000513750.1:p.Ile816Ser
ENST00000698482.1:n.2816T>G
ENST00000698483.1:n.2981T>G
ENST00000698484.1:c.2526T>G	ENSP00000513751.1:p.Asn842Lys
ENST00000698485.1:c.2447T>G	ENSP00000513752.1:p.Ile816Ser
ENST00000698486.1:n.3066T>G
ENST00000698487.1:c.2526T>G	ENSP00000513753.1:p.Asn842Lys
ENST00000698488.1:c.2270T>G	ENSP00000513754.1:p.Ile757Ser
ENST00000698489.1:n.6851T>G
ENST00000698490.1:c.2526T>G	ENSP00000513755.1:p.Asn842Lys
ENST00000698492.1:c.*1241T>G	ENSP00000513756.1:n.*1241T>G
ENST00000698493.1:n.2816T>G
ENST00000698494.1:c.*506T>G	ENSP00000513757.1:n.*506T>G
ENST00000358746.7:c.2526T>G MANE Select	ENSP00000351596.3:p.Asn842Lys
ENST00000649566.1:c.2526T>G	ENSP00000497948.1:p.Asn842Lys
ENST00000358746.6:c.2526T>G	ENSP00000351596.2:p.Asn842Lys
ENST00000506007.1:n.193T>G
ENST00000507805.5:n.798T>G
ENST00000508181.5:n.99T>G
NM_014639.3:c.2526T>G , LRG_173t1:c.2526T>G	NP_055454.1:p.Asn842Lys
XR_948312.1:n.2795T>G
XR_001742370.2:n.2798T>G
NM_014639.4:c.2526T>G MANE Select	NP_055454.1:p.Asn842Lys