Canonical Allele Identifier: CA2016564123
Gene: ETV6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11702690A= , CM000674.2:g.11702690A= GRCh38
NC_000012.11:g.11855624A= , CM000674.1:g.11855624A= GRCh37
NC_000012.10:g.11746891A= NCBI36
NG_011443.1:g.57837A= , LRG_609:g.57837A=

Transcript Alleles

HGVS Amino-acid Change
NM_001987.5:c.34-49760A= MANE Select NP_001978.1:n.34-49760A=
ENST00000396373.9:c.34-49760A= MANE Select ENSP00000379658.3:n.34-49760A=
NM_001987.4:c.34-49760A= , LRG_609t1:c.34-49760A= NP_001978.1:n.34-49760A=
ENST00000396373.8:c.34-49760A= ENSP00000379658.3:n.34-49760A=
ENST00000541426.1:n.218-49760A=
ENST00000544715.1:n.151-13897A=
XM_011520607.1:c.34-49763A= XP_011518909.1:n.34-49763A=
XM_011520607.2:c.34-49763A= XP_011518909.1:n.34-49763A=
XM_011520611.1:c.-102+52530A= XP_011518913.1:n.-102+52530A=
XM_011520611.2:c.-102+52530A= XP_011518913.1:n.-102+52530A=
XM_017018990.1:c.34-49760A= XP_016874479.1:n.34-49760A=
XM_017018991.1:c.-1627-49760A= XP_016874480.1:n.-1627-49760A=