Canonical Allele Identifier: CA6454323

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11869701G>A , CM000674.2:g.11869701G>A	GRCh38
NC_000012.11:g.12022635G>A , CM000674.1:g.12022635G>A	GRCh37
NC_000012.10:g.11913902G>A	NCBI36
NG_011443.1:g.224848G>A , LRG_609:g.224848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.741G>A MANE Select	ENSP00000379658.3:p.Ala247=
ENST00000396373.8:c.741G>A	ENSP00000379658.3:p.Ala247=
NM_001987.4:c.741G>A , LRG_609t1:c.741G>A	NP_001978.1:p.Ala247=
XM_011520607.1:c.738G>A	XP_011518909.1:p.Ala246=
XM_011520608.1:c.714G>A	XP_011518910.1:p.Ala238=
XM_011520609.1:c.477G>A	XP_011518911.1:p.Ala159=
XM_011520610.1:c.477G>A	XP_011518912.1:p.Ala159=
XM_011520611.1:c.477G>A	XP_011518913.1:p.Ala159=
XM_011520612.1:c.120G>A	XP_011518914.1:p.Ala40=
XM_011520607.2:c.738G>A	XP_011518909.1:p.Ala246=
XM_011520608.2:c.714G>A	XP_011518910.1:p.Ala238=
XM_011520609.2:c.477G>A	XP_011518911.1:p.Ala159=
XM_011520611.2:c.477G>A	XP_011518913.1:p.Ala159=
XM_011520612.2:c.120G>A	XP_011518914.1:p.Ala40=
XM_017018990.1:c.606G>A	XP_016874479.1:p.Ala202=
XM_017018991.1:c.477G>A	XP_016874480.1:p.Ala159=
NM_001987.5:c.741G>A MANE Select	NP_001978.1:p.Ala247=