Canonical Allele Identifier: CA6454306

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11869588C>T , CM000674.2:g.11869588C>T	GRCh38
NC_000012.11:g.12022522C>T , CM000674.1:g.12022522C>T	GRCh37
NC_000012.10:g.11913789C>T	NCBI36
NG_011443.1:g.224735C>T , LRG_609:g.224735C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.628C>T MANE Select	ENSP00000379658.3:p.Arg210Cys
ENST00000396373.8:c.628C>T	ENSP00000379658.3:p.Arg210Cys
NM_001987.4:c.628C>T , LRG_609t1:c.628C>T	NP_001978.1:p.Arg210Cys
XM_011520607.1:c.625C>T	XP_011518909.1:p.Arg209Cys
XM_011520608.1:c.601C>T	XP_011518910.1:p.Arg201Cys
XM_011520609.1:c.364C>T	XP_011518911.1:p.Arg122Cys
XM_011520610.1:c.364C>T	XP_011518912.1:p.Arg122Cys
XM_011520611.1:c.364C>T	XP_011518913.1:p.Arg122Cys
XM_011520612.1:c.7C>T	XP_011518914.1:p.Arg3Cys
XM_011520607.2:c.625C>T	XP_011518909.1:p.Arg209Cys
XM_011520608.2:c.601C>T	XP_011518910.1:p.Arg201Cys
XM_011520609.2:c.364C>T	XP_011518911.1:p.Arg122Cys
XM_011520611.2:c.364C>T	XP_011518913.1:p.Arg122Cys
XM_011520612.2:c.7C>T	XP_011518914.1:p.Arg3Cys
XM_017018990.1:c.493C>T	XP_016874479.1:p.Arg165Cys
XM_017018991.1:c.364C>T	XP_016874480.1:p.Arg122Cys
NM_001987.5:c.628C>T MANE Select	NP_001978.1:p.Arg210Cys