Canonical Allele Identifier: CA370856873

Gene: EXTL3

Linked Data

• MyVariant Identifiers: chr8:g.28574217T>C (hg19) ; chr8:g.28716700T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28716700T>C , CM000670.2:g.28716700T>C	GRCh38
NC_000008.10:g.28574217T>C , CM000670.1:g.28574217T>C	GRCh37
NC_000008.9:g.28630136T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696177.1:c.641T>C	ENSP00000512467.1:p.Val214Ala
ENST00000696178.1:c.641T>C	ENSP00000512468.1:p.Val214Ala
ENST00000696179.1:c.641T>C	ENSP00000512469.1:p.Val214Ala
ENST00000696180.1:c.641T>C	ENSP00000512470.1:p.Val214Ala
ENST00000696181.1:c.641T>C	ENSP00000512471.1:p.Val214Ala
ENST00000696182.1:c.-114-14523T>C	ENSP00000512472.1:n.-114-14523T>C
ENST00000696184.1:c.641T>C	ENSP00000512473.1:p.Val214Ala
ENST00000696185.1:n.1274T>C
ENST00000696186.1:c.641T>C	ENSP00000512474.1:p.Val214Ala
ENST00000220562.9:c.641T>C MANE Select	ENSP00000220562.4:p.Val214Ala
ENST00000220562.8:c.641T>C	ENSP00000220562.4:p.Val214Ala
ENST00000519886.5:n.631+634T>C
ENST00000521532.5:c.42+6197T>C	ENSP00000431013.1:n.42+6197T>C
ENST00000522698.1:c.16T>C
ENST00000523149.5:c.28-539T>C	ENSP00000428691.1:n.28-539T>C
NM_001440.3:c.641T>C	NP_001431.1:p.Val214Ala
NR_073468.1:n.188-14523T>C
NR_073469.1:n.763+634T>C
XM_011544440.1:c.641T>C	XP_011542742.1:p.Val214Ala
XM_011544440.3:c.641T>C	XP_011542742.1:p.Val214Ala
XM_024447094.1:c.641T>C	XP_024302862.1:p.Val214Ala
XM_024447095.1:c.641T>C	XP_024302863.1:p.Val214Ala
XM_024447096.1:c.641T>C	XP_024302864.1:p.Val214Ala
NM_001440.4:c.641T>C MANE Select	NP_001431.1:p.Val214Ala
NR_073468.2:n.160-14523T>C
NR_073469.2:n.735+634T>C