Canonical Allele Identifier: CA6454105

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11752491G>A , CM000674.2:g.11752491G>A	GRCh38
NC_000012.11:g.11905425G>A , CM000674.1:g.11905425G>A	GRCh37
NC_000012.10:g.11796692G>A	NCBI36
NG_011443.1:g.107638G>A , LRG_609:g.107638G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001987.5:c.75G>A MANE Select	NP_001978.1:p.Pro25=
ENST00000396373.9:c.75G>A MANE Select	ENSP00000379658.3:p.Pro25=
NM_001987.4:c.75G>A , LRG_609t1:c.75G>A	NP_001978.1:p.Pro25=
ENST00000396373.8:c.75G>A	ENSP00000379658.3:p.Pro25=
ENST00000541426.1:n.259G>A
ENST00000544715.1:n.349G>A
XM_011520607.1:c.72G>A	XP_011518909.1:p.Pro24=
XM_011520607.2:c.72G>A	XP_011518909.1:p.Pro24=
XM_011520608.1:c.48G>A	XP_011518910.1:p.Pro16=
XM_011520608.2:c.48G>A	XP_011518910.1:p.Pro16=
XM_011520611.1:c.-101-86649G>A	XP_011518913.1:n.-101-86649G>A
XM_011520611.2:c.-101-86649G>A	XP_011518913.1:n.-101-86649G>A
XM_017018990.1:c.75G>A	XP_016874479.1:p.Pro25=
XM_017018991.1:c.-1586G>A	XP_016874480.1:n.-1586G>A