Canonical Allele Identifier: CA2016648615
Gene: ETV6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11886030G= , CM000674.2:g.11886030G= GRCh38
NC_000012.11:g.12038964G= , CM000674.1:g.12038964G= GRCh37
NC_000012.10:g.11930231G= NCBI36
NG_011443.1:g.241177G= , LRG_609:g.241177G=

Transcript Alleles

HGVS Amino-acid change
ENST00000396373.9:c.1253+4G= MANE Select ENSP00000379658.3:n.1253+4G=
ENST00000266427.3:c.90+4G=
ENST00000396373.8:c.1253+4G= ENSP00000379658.3:n.1253+4G=
NM_001987.4:c.1253+4G= , LRG_609t1:c.1253+4G= NP_001978.1:n.1253+4G=
XM_011520607.1:c.1250+4G= XP_011518909.1:n.1250+4G=
XM_011520608.1:c.1226+4G= XP_011518910.1:n.1226+4G=
XM_011520609.1:c.989+4G= XP_011518911.1:n.989+4G=
XM_011520610.1:c.989+4G= XP_011518912.1:n.989+4G=
XM_011520611.1:c.989+4G= XP_011518913.1:n.989+4G=
XM_011520612.1:c.632+4G= XP_011518914.1:n.632+4G=
XM_011520607.2:c.1250+4G= XP_011518909.1:n.1250+4G=
XM_011520608.2:c.1226+4G= XP_011518910.1:n.1226+4G=
XM_011520609.2:c.989+4G= XP_011518911.1:n.989+4G=
XM_011520611.2:c.989+4G= XP_011518913.1:n.989+4G=
XM_011520612.2:c.632+4G= XP_011518914.1:n.632+4G=
XM_017018990.1:c.1118+4G= XP_016874479.1:n.1118+4G=
XM_017018991.1:c.989+4G= XP_016874480.1:n.989+4G=
NM_001987.5:c.1253+4G= MANE Select NP_001978.1:n.1253+4G=