Canonical Allele Identifier: CA384044822

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038870A>T (hg19) ; chr12:g.11885936A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885936A>T , CM000674.2:g.11885936A>T	GRCh38
NC_000012.11:g.12038870A>T , CM000674.1:g.12038870A>T	GRCh37
NC_000012.10:g.11930137A>T	NCBI36
NG_011443.1:g.241083A>T , LRG_609:g.241083A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1163A>T MANE Select	ENSP00000379658.3:p.Asn388Ile
ENST00000396373.8:c.1163A>T	ENSP00000379658.3:p.Asn388Ile
NM_001987.4:c.1163A>T , LRG_609t1:c.1163A>T	NP_001978.1:p.Asn388Ile
XM_011520607.1:c.1160A>T	XP_011518909.1:p.Asn387Ile
XM_011520608.1:c.1136A>T	XP_011518910.1:p.Asn379Ile
XM_011520609.1:c.899A>T	XP_011518911.1:p.Asn300Ile
XM_011520610.1:c.899A>T	XP_011518912.1:p.Asn300Ile
XM_011520611.1:c.899A>T	XP_011518913.1:p.Asn300Ile
XM_011520612.1:c.542A>T	XP_011518914.1:p.Asn181Ile
XM_011520607.2:c.1160A>T	XP_011518909.1:p.Asn387Ile
XM_011520608.2:c.1136A>T	XP_011518910.1:p.Asn379Ile
XM_011520609.2:c.899A>T	XP_011518911.1:p.Asn300Ile
XM_011520611.2:c.899A>T	XP_011518913.1:p.Asn300Ile
XM_011520612.2:c.542A>T	XP_011518914.1:p.Asn181Ile
XM_017018990.1:c.1028A>T	XP_016874479.1:p.Asn343Ile
XM_017018991.1:c.899A>T	XP_016874480.1:p.Asn300Ile
NM_001987.5:c.1163A>T MANE Select	NP_001978.1:p.Asn388Ile