Canonical Allele Identifier: CA9526535

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46124019A>C , CM000681.2:g.46124019A>C GRCh38
NC_000019.9:g.46627276A>C , CM000681.1:g.46627276A>C GRCh37
NC_000019.8:g.51319116A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_207393.2:c.217T>G (IGFL3) MANE Select NP_997276.1:p.Cys73Gly
ENST00000341415.3:c.217T>G (IGFL3) MANE Select ENSP00000344860.2:p.Cys73Gly
NM_207393.1:c.217T>G (IGFL3) NP_997276.1:p.Cys73Gly
ENST00000341415.2:c.217T>G (IGFL3) ENSP00000344860.2:p.Cys73Gly
XM_011526502.1:c.-791-19046A>C (IGFL2) XP_011524804.1:n.-791-19046A>C
XM_011526953.1:c.217T>G (IGFL3) XP_011525255.1:p.Cys73Gly
XM_011526953.2:c.217T>G (IGFL3) XP_011525255.1:p.Cys73Gly
XM_017026796.1:c.328T>G (IGFL3) XP_016882285.1:p.Cys110Gly
XM_017026797.2:c.328T>G (IGFL3) XP_016882286.1:p.Cys110Gly
XM_024451381.1:c.-258+22882A>C (IGFL2) XP_024307149.1:n.-258+22882A>C
XR_001753604.1:n.1576-19046A>C (IGFL2)
XR_001753605.1:n.1732+22882A>C (IGFL2)
XR_002958257.1:n.1004+43932A>C (IGFL2)
XR_002958259.1:n.1004+43932A>C (IGFL2)
XR_002958260.1:n.1004+43932A>C (IGFL2)
XR_002958261.1:n.1004+43932A>C (IGFL2)
XR_002958262.1:n.1004+43932A>C (IGFL2)
XR_002958263.1:n.1004+43932A>C (IGFL2)
XR_002958264.1:n.1004+43932A>C (IGFL2)
XR_002958265.1:n.1004+43932A>C (IGFL2)
XR_002958266.1:n.1004+43932A>C (IGFL2)
XR_002958267.1:n.1004+43932A>C (IGFL2)
XR_002958269.1:n.1004+43932A>C (IGFL2)
XR_002958270.1:n.1004+43932A>C (IGFL2)
XR_002958271.1:n.1004+43932A>C (IGFL2)
XR_002958272.1:n.1004+43932A>C (IGFL2)
XR_935742.1:n.1561-36396A>C (IGFL2)
XR_935743.1:n.1561-36396A>C (IGFL2)
XR_935743.2:n.1576-36396A>C (IGFL2)
XR_935744.1:n.1560+43932A>C (IGFL2)
XR_935744.2:n.1575+43932A>C (IGFL2)
XR_935745.1:n.1561-36396A>C (IGFL2)
XR_935746.1:n.1560+43932A>C (IGFL2)