Canonical Allele Identifier: CA2499221459

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11752442T>G , CM000674.2:g.11752442T>G	GRCh38
NC_000012.11:g.11905376T>G , CM000674.1:g.11905376T>G	GRCh37
NC_000012.10:g.11796643T>G	NCBI36
NG_011443.1:g.107589T>G , LRG_609:g.107589T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.34-8T>G MANE Select	ENSP00000379658.3:n.34-8T>G
ENST00000396373.8:c.34-8T>G	ENSP00000379658.3:n.34-8T>G
ENST00000541426.1:n.218-8T>G
ENST00000544715.1:n.308-8T>G
NM_001987.4:c.34-8T>G , LRG_609t1:c.34-8T>G	NP_001978.1:n.34-8T>G
XM_011520607.1:c.34-11T>G	XP_011518909.1:n.34-11T>G
XM_011520608.1:c.7-8T>G	XP_011518910.1:n.7-8T>G
XM_011520611.1:c.-101-86698T>G	XP_011518913.1:n.-101-86698T>G
XM_011520607.2:c.34-11T>G	XP_011518909.1:n.34-11T>G
XM_011520608.2:c.7-8T>G	XP_011518910.1:n.7-8T>G
XM_011520611.2:c.-101-86698T>G	XP_011518913.1:n.-101-86698T>G
XM_017018990.1:c.34-8T>G	XP_016874479.1:n.34-8T>G
XM_017018991.1:c.-1627-8T>G	XP_016874480.1:n.-1627-8T>G
NM_001987.5:c.34-8T>G MANE Select	NP_001978.1:n.34-8T>G