Canonical Allele Identifier: CA370857741
Gene: EXTL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1425538
ClinVar RCV Id: RCV001926720
dbSNP Id: rs2130737942
gnomAD v4: 8-28716955-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28716955C>T , CM000670.2:g.28716955C>T GRCh38
NC_000008.10:g.28574472C>T , CM000670.1:g.28574472C>T GRCh37
NC_000008.9:g.28630391C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696177.1:c.896C>T ENSP00000512467.1:p.Ala299Val
ENST00000696178.1:c.896C>T ENSP00000512468.1:p.Ala299Val
ENST00000696179.1:c.896C>T ENSP00000512469.1:p.Ala299Val
ENST00000696180.1:c.896C>T ENSP00000512470.1:p.Ala299Val
ENST00000696181.1:c.896C>T ENSP00000512471.1:p.Ala299Val
ENST00000696182.1:c.-114-14268C>T ENSP00000512472.1:n.-114-14268C>T
ENST00000696184.1:c.896C>T ENSP00000512473.1:p.Ala299Val
ENST00000696185.1:n.1529C>T
ENST00000696186.1:c.896C>T ENSP00000512474.1:p.Ala299Val
ENST00000220562.9:c.896C>T MANE Select ENSP00000220562.4:p.Ala299Val
ENST00000220562.8:c.896C>T ENSP00000220562.4:p.Ala299Val
ENST00000519886.5:n.631+889C>T
ENST00000521532.5:c.42+6452C>T ENSP00000431013.1:n.42+6452C>T
ENST00000522698.1:c.213+58C>T
ENST00000523149.5:c.28-284C>T ENSP00000428691.1:n.28-284C>T
NM_001440.3:c.896C>T NP_001431.1:p.Ala299Val
NR_073468.1:n.188-14268C>T
NR_073469.1:n.763+889C>T
XM_011544440.1:c.896C>T XP_011542742.1:p.Ala299Val
XM_011544440.3:c.896C>T XP_011542742.1:p.Ala299Val
XM_024447094.1:c.896C>T XP_024302862.1:p.Ala299Val
XM_024447095.1:c.896C>T XP_024302863.1:p.Ala299Val
XM_024447096.1:c.896C>T XP_024302864.1:p.Ala299Val
NM_001440.4:c.896C>T MANE Select NP_001431.1:p.Ala299Val
NR_073468.2:n.160-14268C>T
NR_073469.2:n.735+889C>T