Canonical Allele Identifier: CA6454332

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11869736G>A , CM000674.2:g.11869736G>A	GRCh38
NC_000012.11:g.12022670G>A , CM000674.1:g.12022670G>A	GRCh37
NC_000012.10:g.11913937G>A	NCBI36
NG_011443.1:g.224883G>A , LRG_609:g.224883G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.776G>A MANE Select	ENSP00000379658.3:p.Arg259Gln
ENST00000396373.8:c.776G>A	ENSP00000379658.3:p.Arg259Gln
NM_001987.4:c.776G>A , LRG_609t1:c.776G>A	NP_001978.1:p.Arg259Gln
XM_011520607.1:c.773G>A	XP_011518909.1:p.Arg258Gln
XM_011520608.1:c.749G>A	XP_011518910.1:p.Arg250Gln
XM_011520609.1:c.512G>A	XP_011518911.1:p.Arg171Gln
XM_011520610.1:c.512G>A	XP_011518912.1:p.Arg171Gln
XM_011520611.1:c.512G>A	XP_011518913.1:p.Arg171Gln
XM_011520612.1:c.155G>A	XP_011518914.1:p.Arg52Gln
XM_011520607.2:c.773G>A	XP_011518909.1:p.Arg258Gln
XM_011520608.2:c.749G>A	XP_011518910.1:p.Arg250Gln
XM_011520609.2:c.512G>A	XP_011518911.1:p.Arg171Gln
XM_011520611.2:c.512G>A	XP_011518913.1:p.Arg171Gln
XM_011520612.2:c.155G>A	XP_011518914.1:p.Arg52Gln
XM_017018990.1:c.641G>A	XP_016874479.1:p.Arg214Gln
XM_017018991.1:c.512G>A	XP_016874480.1:p.Arg171Gln
NM_001987.5:c.776G>A MANE Select	NP_001978.1:p.Arg259Gln