Canonical Allele Identifier: CA478767199

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038877C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885943C>A , CM000674.2:g.11885943C>A	GRCh38
NC_000012.11:g.12038877C>A , CM000674.1:g.12038877C>A	GRCh37
NC_000012.10:g.11930144C>A	NCBI36
NG_011443.1:g.241090C>A , LRG_609:g.241090C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1170C>A MANE Select	ENSP00000379658.3:p.Thr390=
ENST00000266427.3:c.7C>A
ENST00000396373.8:c.1170C>A	ENSP00000379658.3:p.Thr390=
NM_001987.4:c.1170C>A , LRG_609t1:c.1170C>A	NP_001978.1:p.Thr390=
XM_011520607.1:c.1167C>A	XP_011518909.1:p.Thr389=
XM_011520608.1:c.1143C>A	XP_011518910.1:p.Thr381=
XM_011520609.1:c.906C>A	XP_011518911.1:p.Thr302=
XM_011520610.1:c.906C>A	XP_011518912.1:p.Thr302=
XM_011520611.1:c.906C>A	XP_011518913.1:p.Thr302=
XM_011520612.1:c.549C>A	XP_011518914.1:p.Thr183=
XM_011520607.2:c.1167C>A	XP_011518909.1:p.Thr389=
XM_011520608.2:c.1143C>A	XP_011518910.1:p.Thr381=
XM_011520609.2:c.906C>A	XP_011518911.1:p.Thr302=
XM_011520611.2:c.906C>A	XP_011518913.1:p.Thr302=
XM_011520612.2:c.549C>A	XP_011518914.1:p.Thr183=
XM_017018990.1:c.1035C>A	XP_016874479.1:p.Thr345=
XM_017018991.1:c.906C>A	XP_016874480.1:p.Thr302=
NM_001987.5:c.1170C>A MANE Select	NP_001978.1:p.Thr390=