Canonical Allele Identifier: CA1396339266
Gene: IGSF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.118957645T>A , CM000665.2:g.118957645T>A GRCh38
NC_000003.11:g.118676492T>A , CM000665.1:g.118676492T>A GRCh37
NC_000003.10:g.120159182T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001015887.3:c.53-27370A>T MANE Select NP_001015887.1:n.53-27370A>T
ENST00000393775.7:c.53-27370A>T MANE Select ENSP00000377370.2:n.53-27370A>T
NM_001015887.1:c.53-27370A>T NP_001015887.1:n.53-27370A>T
NM_001015887.2:c.53-27370A>T NP_001015887.1:n.53-27370A>T
NM_001353318.1:c.202+24146A>T NP_001340247.1:n.202+24146A>T
NM_001353318.2:c.202+24146A>T NP_001340247.1:n.202+24146A>T
NM_001353319.1:c.202+24146A>T NP_001340248.1:n.202+24146A>T
NM_001353319.2:c.202+24146A>T NP_001340248.1:n.202+24146A>T
NM_001353320.1:c.50-27370A>T NP_001340249.1:n.50-27370A>T
NM_001353320.2:c.50-27370A>T NP_001340249.1:n.50-27370A>T
NM_001353321.1:c.53-27370A>T NP_001340250.1:n.53-27370A>T
NM_001353321.2:c.53-27370A>T NP_001340250.1:n.53-27370A>T
NM_001353322.1:c.50-27370A>T NP_001340251.1:n.50-27370A>T
NM_001353322.2:c.50-27370A>T NP_001340251.1:n.50-27370A>T
NM_001353323.1:c.53-27370A>T NP_001340252.1:n.53-27370A>T
NM_001353323.2:c.53-27370A>T NP_001340252.1:n.53-27370A>T
NM_001353324.1:c.53-27370A>T NP_001340253.1:n.53-27370A>T
NM_001353324.2:c.53-27370A>T NP_001340253.1:n.53-27370A>T
NM_001353325.1:c.-215-8327A>T NP_001340254.1:n.-215-8327A>T
NM_001353325.2:c.-215-8327A>T NP_001340254.1:n.-215-8327A>T
NM_001353326.1:c.-215-8327A>T NP_001340255.1:n.-215-8327A>T
NM_001353326.2:c.-215-8327A>T NP_001340255.1:n.-215-8327A>T
NM_152538.2:c.50-27370A>T NP_689751.2:n.50-27370A>T
NM_152538.3:c.50-27370A>T NP_689751.2:n.50-27370A>T
NM_152538.4:c.50-27370A>T NP_689751.2:n.50-27370A>T
ENST00000354673.6:c.50-27370A>T ENSP00000346700.2:n.50-27370A>T
ENST00000393775.6:c.53-27370A>T ENSP00000377370.2:n.53-27370A>T
ENST00000425327.6:c.50-27370A>T ENSP00000406092.2:n.50-27370A>T
ENST00000441144.6:c.50-27370A>T ENSP00000401240.2:n.50-27370A>T
ENST00000480431.5:c.-215-8327A>T ENSP00000418047.1:n.-215-8327A>T
ENST00000483401.5:c.-215-8327A>T ENSP00000418976.1:n.-215-8327A>T
ENST00000489689.5:c.53-27370A>T ENSP00000420486.1:n.53-27370A>T
ENST00000491903.1:c.53-27370A>T ENSP00000417413.1:n.53-27370A>T
ENST00000494802.1:n.349-8327A>T
XM_006713517.1:c.-215-8327A>T XP_006713580.1:n.-215-8327A>T
XM_011512462.1:c.202+24146A>T XP_011510764.1:n.202+24146A>T
XM_011512463.1:c.199+24146A>T XP_011510765.1:n.199+24146A>T
XM_011512464.1:c.199+24146A>T XP_011510766.1:n.199+24146A>T
XM_011512464.2:c.199+24146A>T XP_011510766.1:n.199+24146A>T
XM_011512465.1:c.199+24146A>T XP_011510767.1:n.199+24146A>T
XM_011512465.2:c.199+24146A>T XP_011510767.1:n.199+24146A>T
XM_011512466.1:c.202+24146A>T XP_011510768.1:n.202+24146A>T
XM_011512466.2:c.202+24146A>T XP_011510768.1:n.202+24146A>T
XM_011512467.1:c.202+24146A>T XP_011510769.1:n.202+24146A>T
XM_011512468.1:c.88+24146A>T XP_011510770.1:n.88+24146A>T
XM_011512469.1:c.50-27370A>T XP_011510771.1:n.50-27370A>T
XM_011512470.1:c.50-27370A>T XP_011510772.1:n.50-27370A>T
XM_011512471.1:c.202+24146A>T XP_011510773.1:n.202+24146A>T
XM_011512471.3:c.202+24146A>T XP_011510773.1:n.202+24146A>T
XM_011512472.1:c.50-27370A>T XP_011510774.1:n.50-27370A>T
XM_011512473.1:c.202+24146A>T XP_011510775.1:n.202+24146A>T
XM_011512474.1:c.202+24146A>T XP_011510776.1:n.202+24146A>T
XM_011512474.3:c.202+24146A>T XP_011510776.1:n.202+24146A>T
XM_024453376.1:c.88+24146A>T XP_024309144.1:n.88+24146A>T
XM_024453377.1:c.202+24146A>T XP_024309145.1:n.202+24146A>T