Canonical Allele Identifier: CA1773391612

Gene: EXTL3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28716951G= , CM000670.2:g.28716951G=	GRCh38
NC_000008.10:g.28574468G= , CM000670.1:g.28574468G=	GRCh37
NC_000008.9:g.28630387G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.892G=	ENSP00000512467.1:p.Val298=
ENST00000696178.1:c.892G=	ENSP00000512468.1:p.Val298=
ENST00000696179.1:c.892G=	ENSP00000512469.1:p.Val298=
ENST00000696180.1:c.892G=	ENSP00000512470.1:p.Val298=
ENST00000696181.1:c.892G=	ENSP00000512471.1:p.Val298=
ENST00000696182.1:c.-114-14272G=	ENSP00000512472.1:n.-114-14272G=
ENST00000696184.1:c.892G=	ENSP00000512473.1:p.Val298=
ENST00000696185.1:n.1525G=
ENST00000696186.1:c.892G=	ENSP00000512474.1:p.Val298=
ENST00000220562.9:c.892G= MANE Select	ENSP00000220562.4:p.Val298=
ENST00000220562.8:c.892G=	ENSP00000220562.4:p.Val298=
ENST00000519886.5:n.631+885G=
ENST00000521532.5:c.42+6448G=	ENSP00000431013.1:n.42+6448G=
ENST00000522698.1:c.213+54G=
ENST00000523149.5:c.28-288G=	ENSP00000428691.1:n.28-288G=
NM_001440.3:c.892G=	NP_001431.1:p.Val298=
NR_073468.1:n.188-14272G=
NR_073469.1:n.763+885G=
XM_011544440.1:c.892G=	XP_011542742.1:p.Val298=
XM_011544440.3:c.892G=	XP_011542742.1:p.Val298=
XM_024447094.1:c.892G=	XP_024302862.1:p.Val298=
XM_024447095.1:c.892G=	XP_024302863.1:p.Val298=
XM_024447096.1:c.892G=	XP_024302864.1:p.Val298=
NM_001440.4:c.892G= MANE Select	NP_001431.1:p.Val298=
NR_073468.2:n.160-14272G=
NR_073469.2:n.735+885G=