Canonical Allele Identifier: CA6454107

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11752497C>T , CM000674.2:g.11752497C>T	GRCh38
NC_000012.11:g.11905431C>T , CM000674.1:g.11905431C>T	GRCh37
NC_000012.10:g.11796698C>T	NCBI36
NG_011443.1:g.107644C>T , LRG_609:g.107644C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.81C>T MANE Select	ENSP00000379658.3:p.Tyr27=
ENST00000396373.8:c.81C>T	ENSP00000379658.3:p.Tyr27=
ENST00000541426.1:n.265C>T
ENST00000544715.1:n.355C>T
NM_001987.4:c.81C>T , LRG_609t1:c.81C>T	NP_001978.1:p.Tyr27=
XM_011520607.1:c.78C>T	XP_011518909.1:p.Tyr26=
XM_011520608.1:c.54C>T	XP_011518910.1:p.Tyr18=
XM_011520611.1:c.-101-86643C>T	XP_011518913.1:n.-101-86643C>T
XM_011520607.2:c.78C>T	XP_011518909.1:p.Tyr26=
XM_011520608.2:c.54C>T	XP_011518910.1:p.Tyr18=
XM_011520611.2:c.-101-86643C>T	XP_011518913.1:n.-101-86643C>T
XM_017018990.1:c.81C>T	XP_016874479.1:p.Tyr27=
XM_017018991.1:c.-1580C>T	XP_016874480.1:n.-1580C>T
NM_001987.5:c.81C>T MANE Select	NP_001978.1:p.Tyr27=