Canonical Allele Identifier: CA384044554

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11884487A>G , CM000674.2:g.11884487A>G	GRCh38
NC_000012.11:g.12037421A>G , CM000674.1:g.12037421A>G	GRCh37
NC_000012.10:g.11928688A>G	NCBI36
NG_011443.1:g.239634A>G , LRG_609:g.239634A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001987.5:c.1052A>G MANE Select	NP_001978.1:p.Asp351Gly
ENST00000396373.9:c.1052A>G MANE Select	ENSP00000379658.3:p.Asp351Gly
NM_001987.4:c.1052A>G , LRG_609t1:c.1052A>G	NP_001978.1:p.Asp351Gly
ENST00000396373.8:c.1052A>G	ENSP00000379658.3:p.Asp351Gly
XM_011520607.1:c.1049A>G	XP_011518909.1:p.Asp350Gly
XM_011520607.2:c.1049A>G	XP_011518909.1:p.Asp350Gly
XM_011520608.1:c.1025A>G	XP_011518910.1:p.Asp342Gly
XM_011520608.2:c.1025A>G	XP_011518910.1:p.Asp342Gly
XM_011520609.1:c.788A>G	XP_011518911.1:p.Asp263Gly
XM_011520609.2:c.788A>G	XP_011518911.1:p.Asp263Gly
XM_011520610.1:c.788A>G	XP_011518912.1:p.Asp263Gly
XM_011520611.1:c.788A>G	XP_011518913.1:p.Asp263Gly
XM_011520611.2:c.788A>G	XP_011518913.1:p.Asp263Gly
XM_011520612.1:c.431A>G	XP_011518914.1:p.Asp144Gly
XM_011520612.2:c.431A>G	XP_011518914.1:p.Asp144Gly
XM_017018990.1:c.917A>G	XP_016874479.1:p.Asp306Gly
XM_017018991.1:c.788A>G	XP_016874480.1:p.Asp263Gly