Canonical Allele Identifier: CA384044945
Gene: ETV6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11885988C>A , CM000674.2:g.11885988C>A GRCh38
NC_000012.11:g.12038922C>A , CM000674.1:g.12038922C>A GRCh37
NC_000012.10:g.11930189C>A NCBI36
NG_011443.1:g.241135C>A , LRG_609:g.241135C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.1215C>A MANE Select ENSP00000379658.3:p.Asn405Lys
ENST00000266427.3:c.52C>A
ENST00000396373.8:c.1215C>A ENSP00000379658.3:p.Asn405Lys
NM_001987.4:c.1215C>A , LRG_609t1:c.1215C>A NP_001978.1:p.Asn405Lys
XM_011520607.1:c.1212C>A XP_011518909.1:p.Asn404Lys
XM_011520608.1:c.1188C>A XP_011518910.1:p.Asn396Lys
XM_011520609.1:c.951C>A XP_011518911.1:p.Asn317Lys
XM_011520610.1:c.951C>A XP_011518912.1:p.Asn317Lys
XM_011520611.1:c.951C>A XP_011518913.1:p.Asn317Lys
XM_011520612.1:c.594C>A XP_011518914.1:p.Asn198Lys
XM_011520607.2:c.1212C>A XP_011518909.1:p.Asn404Lys
XM_011520608.2:c.1188C>A XP_011518910.1:p.Asn396Lys
XM_011520609.2:c.951C>A XP_011518911.1:p.Asn317Lys
XM_011520611.2:c.951C>A XP_011518913.1:p.Asn317Lys
XM_011520612.2:c.594C>A XP_011518914.1:p.Asn198Lys
XM_017018990.1:c.1080C>A XP_016874479.1:p.Asn360Lys
XM_017018991.1:c.951C>A XP_016874480.1:p.Asn317Lys
NM_001987.5:c.1215C>A MANE Select NP_001978.1:p.Asn405Lys