Canonical Allele Identifier: CA370856917

Gene: EXTL3

Linked Data

• MyVariant Identifiers: chr8:g.28574228T>G (hg19) ; chr8:g.28716711T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28716711T>G , CM000670.2:g.28716711T>G	GRCh38
NC_000008.10:g.28574228T>G , CM000670.1:g.28574228T>G	GRCh37
NC_000008.9:g.28630147T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.652T>G	ENSP00000512467.1:p.Phe218Val
ENST00000696178.1:c.652T>G	ENSP00000512468.1:p.Phe218Val
ENST00000696179.1:c.652T>G	ENSP00000512469.1:p.Phe218Val
ENST00000696180.1:c.652T>G	ENSP00000512470.1:p.Phe218Val
ENST00000696181.1:c.652T>G	ENSP00000512471.1:p.Phe218Val
ENST00000696182.1:c.-114-14512T>G	ENSP00000512472.1:n.-114-14512T>G
ENST00000696184.1:c.652T>G	ENSP00000512473.1:p.Phe218Val
ENST00000696185.1:n.1285T>G
ENST00000696186.1:c.652T>G	ENSP00000512474.1:p.Phe218Val
ENST00000220562.9:c.652T>G MANE Select	ENSP00000220562.4:p.Phe218Val
ENST00000220562.8:c.652T>G	ENSP00000220562.4:p.Phe218Val
ENST00000519886.5:n.631+645T>G
ENST00000521532.5:c.42+6208T>G	ENSP00000431013.1:n.42+6208T>G
ENST00000522698.1:c.27T>G
ENST00000523149.5:c.28-528T>G	ENSP00000428691.1:n.28-528T>G
NM_001440.3:c.652T>G	NP_001431.1:p.Phe218Val
NR_073468.1:n.188-14512T>G
NR_073469.1:n.763+645T>G
XM_011544440.1:c.652T>G	XP_011542742.1:p.Phe218Val
XM_011544440.3:c.652T>G	XP_011542742.1:p.Phe218Val
XM_024447094.1:c.652T>G	XP_024302862.1:p.Phe218Val
XM_024447095.1:c.652T>G	XP_024302863.1:p.Phe218Val
XM_024447096.1:c.652T>G	XP_024302864.1:p.Phe218Val
NM_001440.4:c.652T>G MANE Select	NP_001431.1:p.Phe218Val
NR_073468.2:n.160-14512T>G
NR_073469.2:n.735+645T>G