Canonical Allele Identifier: CA370857775

Gene: EXTL3

Linked Data

• gnomAD v4: 8-28716966-T-A
• MyVariant Identifiers: chr8:g.28574483T>A (hg19) ; chr8:g.28716966T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28716966T>A , CM000670.2:g.28716966T>A	GRCh38
NC_000008.10:g.28574483T>A , CM000670.1:g.28574483T>A	GRCh37
NC_000008.9:g.28630402T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.907T>A	ENSP00000512467.1:p.Phe303Ile
ENST00000696178.1:c.907T>A	ENSP00000512468.1:p.Phe303Ile
ENST00000696179.1:c.907T>A	ENSP00000512469.1:p.Phe303Ile
ENST00000696180.1:c.907T>A	ENSP00000512470.1:p.Phe303Ile
ENST00000696181.1:c.907T>A	ENSP00000512471.1:p.Phe303Ile
ENST00000696182.1:c.-114-14257T>A	ENSP00000512472.1:n.-114-14257T>A
ENST00000696184.1:c.907T>A	ENSP00000512473.1:p.Phe303Ile
ENST00000696185.1:n.1540T>A
ENST00000696186.1:c.907T>A	ENSP00000512474.1:p.Phe303Ile
ENST00000220562.9:c.907T>A MANE Select	ENSP00000220562.4:p.Phe303Ile
ENST00000220562.8:c.907T>A	ENSP00000220562.4:p.Phe303Ile
ENST00000519886.5:n.631+900T>A
ENST00000521532.5:c.42+6463T>A	ENSP00000431013.1:n.42+6463T>A
ENST00000522698.1:c.213+69T>A
ENST00000523149.5:c.28-273T>A	ENSP00000428691.1:n.28-273T>A
NM_001440.3:c.907T>A	NP_001431.1:p.Phe303Ile
NR_073468.1:n.188-14257T>A
NR_073469.1:n.763+900T>A
XM_011544440.1:c.907T>A	XP_011542742.1:p.Phe303Ile
XM_011544440.3:c.907T>A	XP_011542742.1:p.Phe303Ile
XM_024447094.1:c.907T>A	XP_024302862.1:p.Phe303Ile
XM_024447095.1:c.907T>A	XP_024302863.1:p.Phe303Ile
XM_024447096.1:c.907T>A	XP_024302864.1:p.Phe303Ile
NM_001440.4:c.907T>A MANE Select	NP_001431.1:p.Phe303Ile
NR_073468.2:n.160-14257T>A
NR_073469.2:n.735+900T>A