Canonical Allele Identifier: CA1773391574
Gene: EXTL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28716918C= , CM000670.2:g.28716918C= GRCh38
NC_000008.10:g.28574435C= , CM000670.1:g.28574435C= GRCh37
NC_000008.9:g.28630354C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696177.1:c.859C= ENSP00000512467.1:p.Leu287=
ENST00000696178.1:c.859C= ENSP00000512468.1:p.Leu287=
ENST00000696179.1:c.859C= ENSP00000512469.1:p.Leu287=
ENST00000696180.1:c.859C= ENSP00000512470.1:p.Leu287=
ENST00000696181.1:c.859C= ENSP00000512471.1:p.Leu287=
ENST00000696182.1:c.-114-14305C= ENSP00000512472.1:n.-114-14305C=
ENST00000696184.1:c.859C= ENSP00000512473.1:p.Leu287=
ENST00000696185.1:n.1492C=
ENST00000696186.1:c.859C= ENSP00000512474.1:p.Leu287=
ENST00000220562.9:c.859C= MANE Select ENSP00000220562.4:p.Leu287=
ENST00000220562.8:c.859C= ENSP00000220562.4:p.Leu287=
ENST00000519886.5:n.631+852C=
ENST00000521532.5:c.42+6415C= ENSP00000431013.1:n.42+6415C=
ENST00000522698.1:c.213+21C=
ENST00000523149.5:c.28-321C= ENSP00000428691.1:n.28-321C=
NM_001440.3:c.859C= NP_001431.1:p.Leu287=
NR_073468.1:n.188-14305C=
NR_073469.1:n.763+852C=
XM_011544440.1:c.859C= XP_011542742.1:p.Leu287=
XM_011544440.3:c.859C= XP_011542742.1:p.Leu287=
XM_024447094.1:c.859C= XP_024302862.1:p.Leu287=
XM_024447095.1:c.859C= XP_024302863.1:p.Leu287=
XM_024447096.1:c.859C= XP_024302864.1:p.Leu287=
NM_001440.4:c.859C= MANE Select NP_001431.1:p.Leu287=
NR_073468.2:n.160-14305C=
NR_073469.2:n.735+852C=