Canonical Allele Identifier: CA460189471

Gene: EXTL3

Linked Data

• ClinVar Variation Id: 2975393
• ClinVar RCV Id: RCV003830999
• gnomAD v4: 8-28717142-C-T
• MyVariant Identifiers: chr8:g.28574659C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28717142C>T , CM000670.2:g.28717142C>T	GRCh38
NC_000008.10:g.28574659C>T , CM000670.1:g.28574659C>T	GRCh37
NC_000008.9:g.28630578C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.1083C>T	ENSP00000512467.1:p.Arg361=
ENST00000696178.1:c.1083C>T	ENSP00000512468.1:p.Arg361=
ENST00000696179.1:c.1083C>T	ENSP00000512469.1:p.Arg361=
ENST00000696180.1:c.1083C>T	ENSP00000512470.1:p.Arg361=
ENST00000696181.1:c.1083C>T	ENSP00000512471.1:p.Arg361=
ENST00000696182.1:c.-114-14081C>T	ENSP00000512472.1:n.-114-14081C>T
ENST00000696184.1:c.1083C>T	ENSP00000512473.1:p.Arg361=
ENST00000696185.1:n.1716C>T
ENST00000696186.1:c.1083C>T	ENSP00000512474.1:p.Arg361=
ENST00000220562.9:c.1083C>T MANE Select	ENSP00000220562.4:p.Arg361=
ENST00000220562.8:c.1083C>T	ENSP00000220562.4:p.Arg361=
ENST00000519886.5:n.631+1076C>T
ENST00000521532.5:c.42+6639C>T	ENSP00000431013.1:n.42+6639C>T
ENST00000522698.1:c.213+245C>T
ENST00000523149.5:c.28-97C>T	ENSP00000428691.1:n.28-97C>T
NM_001440.3:c.1083C>T	NP_001431.1:p.Arg361=
NR_073468.1:n.188-14081C>T
NR_073469.1:n.763+1076C>T
XM_011544440.1:c.1083C>T	XP_011542742.1:p.Arg361=
XM_011544440.3:c.1083C>T	XP_011542742.1:p.Arg361=
XM_024447094.1:c.1083C>T	XP_024302862.1:p.Arg361=
XM_024447095.1:c.1083C>T	XP_024302863.1:p.Arg361=
XM_024447096.1:c.1083C>T	XP_024302864.1:p.Arg361=
NM_001440.4:c.1083C>T MANE Select	NP_001431.1:p.Arg361=
NR_073468.2:n.160-14081C>T
NR_073469.2:n.735+1076C>T