Canonical Allele Identifier: CA384044891

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885963C>T , CM000674.2:g.11885963C>T	GRCh38
NC_000012.11:g.12038897C>T , CM000674.1:g.12038897C>T	GRCh37
NC_000012.10:g.11930164C>T	NCBI36
NG_011443.1:g.241110C>T , LRG_609:g.241110C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1190C>T MANE Select	ENSP00000379658.3:p.Ala397Val
ENST00000266427.3:c.27C>T
ENST00000396373.8:c.1190C>T	ENSP00000379658.3:p.Ala397Val
NM_001987.4:c.1190C>T , LRG_609t1:c.1190C>T	NP_001978.1:p.Ala397Val
XM_011520607.1:c.1187C>T	XP_011518909.1:p.Ala396Val
XM_011520608.1:c.1163C>T	XP_011518910.1:p.Ala388Val
XM_011520609.1:c.926C>T	XP_011518911.1:p.Ala309Val
XM_011520610.1:c.926C>T	XP_011518912.1:p.Ala309Val
XM_011520611.1:c.926C>T	XP_011518913.1:p.Ala309Val
XM_011520612.1:c.569C>T	XP_011518914.1:p.Ala190Val
XM_011520607.2:c.1187C>T	XP_011518909.1:p.Ala396Val
XM_011520608.2:c.1163C>T	XP_011518910.1:p.Ala388Val
XM_011520609.2:c.926C>T	XP_011518911.1:p.Ala309Val
XM_011520611.2:c.926C>T	XP_011518913.1:p.Ala309Val
XM_011520612.2:c.569C>T	XP_011518914.1:p.Ala190Val
XM_017018990.1:c.1055C>T	XP_016874479.1:p.Ala352Val
XM_017018991.1:c.926C>T	XP_016874480.1:p.Ala309Val
NM_001987.5:c.1190C>T MANE Select	NP_001978.1:p.Ala397Val