Canonical Allele Identifier: CA384045027

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038956T>A (hg19) ; chr12:g.11886022T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886022T>A , CM000674.2:g.11886022T>A	GRCh38
NC_000012.11:g.12038956T>A , CM000674.1:g.12038956T>A	GRCh37
NC_000012.10:g.11930223T>A	NCBI36
NG_011443.1:g.241169T>A , LRG_609:g.241169T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1249T>A MANE Select	ENSP00000379658.3:p.Phe417Ile
ENST00000266427.3:c.86T>A
ENST00000396373.8:c.1249T>A	ENSP00000379658.3:p.Phe417Ile
NM_001987.4:c.1249T>A , LRG_609t1:c.1249T>A	NP_001978.1:p.Phe417Ile
XM_011520607.1:c.1246T>A	XP_011518909.1:p.Phe416Ile
XM_011520608.1:c.1222T>A	XP_011518910.1:p.Phe408Ile
XM_011520609.1:c.985T>A	XP_011518911.1:p.Phe329Ile
XM_011520610.1:c.985T>A	XP_011518912.1:p.Phe329Ile
XM_011520611.1:c.985T>A	XP_011518913.1:p.Phe329Ile
XM_011520612.1:c.628T>A	XP_011518914.1:p.Phe210Ile
XM_011520607.2:c.1246T>A	XP_011518909.1:p.Phe416Ile
XM_011520608.2:c.1222T>A	XP_011518910.1:p.Phe408Ile
XM_011520609.2:c.985T>A	XP_011518911.1:p.Phe329Ile
XM_011520611.2:c.985T>A	XP_011518913.1:p.Phe329Ile
XM_011520612.2:c.628T>A	XP_011518914.1:p.Phe210Ile
XM_017018990.1:c.1114T>A	XP_016874479.1:p.Phe372Ile
XM_017018991.1:c.985T>A	XP_016874480.1:p.Phe329Ile
NM_001987.5:c.1249T>A MANE Select	NP_001978.1:p.Phe417Ile