Canonical Allele Identifier: CA384044950

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038924T>A (hg19) ; chr12:g.11885990T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885990T>A , CM000674.2:g.11885990T>A	GRCh38
NC_000012.11:g.12038924T>A , CM000674.1:g.12038924T>A	GRCh37
NC_000012.10:g.11930191T>A	NCBI36
NG_011443.1:g.241137T>A , LRG_609:g.241137T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1217T>A MANE Select	ENSP00000379658.3:p.Ile406Asn
ENST00000266427.3:c.54T>A
ENST00000396373.8:c.1217T>A	ENSP00000379658.3:p.Ile406Asn
NM_001987.4:c.1217T>A , LRG_609t1:c.1217T>A	NP_001978.1:p.Ile406Asn
XM_011520607.1:c.1214T>A	XP_011518909.1:p.Ile405Asn
XM_011520608.1:c.1190T>A	XP_011518910.1:p.Ile397Asn
XM_011520609.1:c.953T>A	XP_011518911.1:p.Ile318Asn
XM_011520610.1:c.953T>A	XP_011518912.1:p.Ile318Asn
XM_011520611.1:c.953T>A	XP_011518913.1:p.Ile318Asn
XM_011520612.1:c.596T>A	XP_011518914.1:p.Ile199Asn
XM_011520607.2:c.1214T>A	XP_011518909.1:p.Ile405Asn
XM_011520608.2:c.1190T>A	XP_011518910.1:p.Ile397Asn
XM_011520609.2:c.953T>A	XP_011518911.1:p.Ile318Asn
XM_011520611.2:c.953T>A	XP_011518913.1:p.Ile318Asn
XM_011520612.2:c.596T>A	XP_011518914.1:p.Ile199Asn
XM_017018990.1:c.1082T>A	XP_016874479.1:p.Ile361Asn
XM_017018991.1:c.953T>A	XP_016874480.1:p.Ile318Asn
NM_001987.5:c.1217T>A MANE Select	NP_001978.1:p.Ile406Asn