Canonical Allele Identifier: CA460188998

Gene: EXTL3

Linked Data

• ClinVar Variation Id: 1655443
• ClinVar RCV Id: RCV002166603
• dbSNP Id: rs1477625189
• gnomAD v4: 8-28716998-C-T
• MyVariant Identifiers: chr8:g.28574515C>T (hg19) ; chr8:g.28716998C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28716998C>T , CM000670.2:g.28716998C>T	GRCh38
NC_000008.10:g.28574515C>T , CM000670.1:g.28574515C>T	GRCh37
NC_000008.9:g.28630434C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.939C>T	ENSP00000512467.1:p.Asp313=
ENST00000696178.1:c.939C>T	ENSP00000512468.1:p.Asp313=
ENST00000696179.1:c.939C>T	ENSP00000512469.1:p.Asp313=
ENST00000696180.1:c.939C>T	ENSP00000512470.1:p.Asp313=
ENST00000696181.1:c.939C>T	ENSP00000512471.1:p.Asp313=
ENST00000696182.1:c.-114-14225C>T	ENSP00000512472.1:n.-114-14225C>T
ENST00000696184.1:c.939C>T	ENSP00000512473.1:p.Asp313=
ENST00000696185.1:n.1572C>T
ENST00000696186.1:c.939C>T	ENSP00000512474.1:p.Asp313=
ENST00000220562.9:c.939C>T MANE Select	ENSP00000220562.4:p.Asp313=
ENST00000220562.8:c.939C>T	ENSP00000220562.4:p.Asp313=
ENST00000519886.5:n.631+932C>T
ENST00000521532.5:c.42+6495C>T	ENSP00000431013.1:n.42+6495C>T
ENST00000522698.1:c.213+101C>T
ENST00000523149.5:c.28-241C>T	ENSP00000428691.1:n.28-241C>T
NM_001440.3:c.939C>T	NP_001431.1:p.Asp313=
NR_073468.1:n.188-14225C>T
NR_073469.1:n.763+932C>T
XM_011544440.1:c.939C>T	XP_011542742.1:p.Asp313=
XM_011544440.3:c.939C>T	XP_011542742.1:p.Asp313=
XM_024447094.1:c.939C>T	XP_024302862.1:p.Asp313=
XM_024447095.1:c.939C>T	XP_024302863.1:p.Asp313=
XM_024447096.1:c.939C>T	XP_024302864.1:p.Asp313=
NM_001440.4:c.939C>T MANE Select	NP_001431.1:p.Asp313=
NR_073468.2:n.160-14225C>T
NR_073469.2:n.735+932C>T