Canonical Allele Identifier: CA6454354
Gene: ETV6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11869865A>G , CM000674.2:g.11869865A>G GRCh38
NC_000012.11:g.12022799A>G , CM000674.1:g.12022799A>G GRCh37
NC_000012.10:g.11914066A>G NCBI36
NG_011443.1:g.225012A>G , LRG_609:g.225012A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.905A>G MANE Select ENSP00000379658.3:p.Lys302Arg
ENST00000396373.8:c.905A>G ENSP00000379658.3:p.Lys302Arg
NM_001987.4:c.905A>G , LRG_609t1:c.905A>G NP_001978.1:p.Lys302Arg
XM_011520607.1:c.902A>G XP_011518909.1:p.Lys301Arg
XM_011520608.1:c.878A>G XP_011518910.1:p.Lys293Arg
XM_011520609.1:c.641A>G XP_011518911.1:p.Lys214Arg
XM_011520610.1:c.641A>G XP_011518912.1:p.Lys214Arg
XM_011520611.1:c.641A>G XP_011518913.1:p.Lys214Arg
XM_011520612.1:c.284A>G XP_011518914.1:p.Lys95Arg
XM_011520607.2:c.902A>G XP_011518909.1:p.Lys301Arg
XM_011520608.2:c.878A>G XP_011518910.1:p.Lys293Arg
XM_011520609.2:c.641A>G XP_011518911.1:p.Lys214Arg
XM_011520611.2:c.641A>G XP_011518913.1:p.Lys214Arg
XM_011520612.2:c.284A>G XP_011518914.1:p.Lys95Arg
XM_017018990.1:c.770A>G XP_016874479.1:p.Lys257Arg
XM_017018991.1:c.641A>G XP_016874480.1:p.Lys214Arg
NM_001987.5:c.905A>G MANE Select NP_001978.1:p.Lys302Arg