Canonical Allele Identifier: CA360457859

Gene: SKIC3

Linked Data

• gnomAD v4: 5-95516574-T-C
• MyVariant Identifiers: chr5:g.94852278T>C (hg19) ; chr5:g.95516574T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95516574T>C , CM000667.2:g.95516574T>C	GRCh38
NC_000005.9:g.94852278T>C , CM000667.1:g.94852278T>C	GRCh37
NC_000005.8:g.94878034T>C	NCBI36
NG_023414.1:g.43432A>G , LRG_173:g.43432A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000506007.2:n.3068A>G
ENST00000513232.2:c.*1493A>G	ENSP00000422749.2:n.*1493A>G
ENST00000698450.1:n.1912A>G
ENST00000698451.1:n.2198A>G
ENST00000698452.1:n.3269A>G
ENST00000698453.1:c.2454A>G	ENSP00000513735.1:p.Leu818=
ENST00000698454.1:c.2519A>G	ENSP00000513736.1:p.Tyr840Cys
ENST00000698455.1:c.*2754A>G	ENSP00000513737.1:n.*2754A>G
ENST00000698456.1:c.*1386A>G	ENSP00000513738.1:n.*1386A>G
ENST00000698457.1:c.2318A>G	ENSP00000513739.1:p.Tyr773Cys
ENST00000698458.1:c.2490A>G	ENSP00000513740.1:p.Leu830=
ENST00000698459.1:c.2528A>G	ENSP00000513741.1:p.Tyr843Cys
ENST00000698460.1:c.*291A>G	ENSP00000513742.1:n.*291A>G
ENST00000698461.1:n.2983A>G
ENST00000698462.1:n.2903A>G
ENST00000698468.1:n.3269A>G
ENST00000698469.1:c.*2125A>G	ENSP00000513743.1:n.*2125A>G
ENST00000698470.1:c.*620A>G	ENSP00000513744.1:n.*620A>G
ENST00000698471.1:n.3068A>G
ENST00000698472.1:c.*1493A>G	ENSP00000513745.1:n.*1493A>G
ENST00000698473.1:n.3068A>G
ENST00000698474.1:n.3068A>G
ENST00000698475.1:n.3153A>G
ENST00000698476.1:c.2528A>G	ENSP00000513746.1:p.Tyr843Cys
ENST00000698477.1:c.2454A>G	ENSP00000513747.1:p.Leu818=
ENST00000698478.1:n.3068A>G
ENST00000698479.1:c.2528A>G	ENSP00000513748.1:p.Tyr843Cys
ENST00000698480.1:c.2449A>G	ENSP00000513749.1:p.Met817Val
ENST00000698481.1:c.2449A>G	ENSP00000513750.1:p.Met817Val
ENST00000698482.1:n.2818A>G
ENST00000698483.1:n.2983A>G
ENST00000698484.1:c.2528A>G	ENSP00000513751.1:p.Tyr843Cys
ENST00000698485.1:c.2449A>G	ENSP00000513752.1:p.Met817Val
ENST00000698486.1:n.3068A>G
ENST00000698487.1:c.2528A>G	ENSP00000513753.1:p.Tyr843Cys
ENST00000698488.1:c.2272A>G	ENSP00000513754.1:p.Met758Val
ENST00000698489.1:n.6853A>G
ENST00000698490.1:c.2528A>G	ENSP00000513755.1:p.Tyr843Cys
ENST00000698492.1:c.*1243A>G	ENSP00000513756.1:n.*1243A>G
ENST00000698493.1:n.2818A>G
ENST00000698494.1:c.*508A>G	ENSP00000513757.1:n.*508A>G
ENST00000358746.7:c.2528A>G MANE Select	ENSP00000351596.3:p.Tyr843Cys
ENST00000649566.1:c.2528A>G	ENSP00000497948.1:p.Tyr843Cys
ENST00000358746.6:c.2528A>G	ENSP00000351596.2:p.Tyr843Cys
ENST00000506007.1:n.195A>G
ENST00000507805.5:n.800A>G
ENST00000508181.5:n.101A>G
NM_014639.3:c.2528A>G , LRG_173t1:c.2528A>G	NP_055454.1:p.Tyr843Cys
XR_948312.1:n.2797A>G
XR_001742370.2:n.2800A>G
NM_014639.4:c.2528A>G MANE Select	NP_055454.1:p.Tyr843Cys