Canonical Allele Identifier: CA4696127

Gene: EXTL3

Linked Data

• ClinVar Variation Id: 1950593
• ClinVar RCV Id: RCV002681353
• dbSNP Id: rs760747701
• ExAC: 8:28574638 G / A
• gnomAD v2: 8-28574638-G-A
• gnomAD v3: 8-28717121-G-A
• gnomAD v4: 8-28717121-G-A
• MyVariant Identifiers: chr8:g.28574638G>A (hg19) ; chr8:g.28717121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28717121G>A , CM000670.2:g.28717121G>A	GRCh38
NC_000008.10:g.28574638G>A , CM000670.1:g.28574638G>A	GRCh37
NC_000008.9:g.28630557G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.1062G>A	ENSP00000512467.1:p.Arg354=
ENST00000696178.1:c.1062G>A	ENSP00000512468.1:p.Arg354=
ENST00000696179.1:c.1062G>A	ENSP00000512469.1:p.Arg354=
ENST00000696180.1:c.1062G>A	ENSP00000512470.1:p.Arg354=
ENST00000696181.1:c.1062G>A	ENSP00000512471.1:p.Arg354=
ENST00000696182.1:c.-114-14102G>A	ENSP00000512472.1:n.-114-14102G>A
ENST00000696184.1:c.1062G>A	ENSP00000512473.1:p.Arg354=
ENST00000696185.1:n.1695G>A
ENST00000696186.1:c.1062G>A	ENSP00000512474.1:p.Arg354=
ENST00000220562.9:c.1062G>A MANE Select	ENSP00000220562.4:p.Arg354=
ENST00000220562.8:c.1062G>A	ENSP00000220562.4:p.Arg354=
ENST00000519886.5:n.631+1055G>A
ENST00000521532.5:c.42+6618G>A	ENSP00000431013.1:n.42+6618G>A
ENST00000522698.1:c.213+224G>A
ENST00000523149.5:c.28-118G>A	ENSP00000428691.1:n.28-118G>A
NM_001440.3:c.1062G>A	NP_001431.1:p.Arg354=
NR_073468.1:n.188-14102G>A
NR_073469.1:n.763+1055G>A
XM_011544440.1:c.1062G>A	XP_011542742.1:p.Arg354=
XM_011544440.3:c.1062G>A	XP_011542742.1:p.Arg354=
XM_024447094.1:c.1062G>A	XP_024302862.1:p.Arg354=
XM_024447095.1:c.1062G>A	XP_024302863.1:p.Arg354=
XM_024447096.1:c.1062G>A	XP_024302864.1:p.Arg354=
NM_001440.4:c.1062G>A MANE Select	NP_001431.1:p.Arg354=
NR_073468.2:n.160-14102G>A
NR_073469.2:n.735+1055G>A