Canonical Allele Identifier: CA384045008

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038948G>T (hg19) ; chr12:g.11886014G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886014G>T , CM000674.2:g.11886014G>T	GRCh38
NC_000012.11:g.12038948G>T , CM000674.1:g.12038948G>T	GRCh37
NC_000012.10:g.11930215G>T	NCBI36
NG_011443.1:g.241161G>T , LRG_609:g.241161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1241G>T MANE Select	ENSP00000379658.3:p.Arg414Met
ENST00000266427.3:c.78G>T
ENST00000396373.8:c.1241G>T	ENSP00000379658.3:p.Arg414Met
NM_001987.4:c.1241G>T , LRG_609t1:c.1241G>T	NP_001978.1:p.Arg414Met
XM_011520607.1:c.1238G>T	XP_011518909.1:p.Arg413Met
XM_011520608.1:c.1214G>T	XP_011518910.1:p.Arg405Met
XM_011520609.1:c.977G>T	XP_011518911.1:p.Arg326Met
XM_011520610.1:c.977G>T	XP_011518912.1:p.Arg326Met
XM_011520611.1:c.977G>T	XP_011518913.1:p.Arg326Met
XM_011520612.1:c.620G>T	XP_011518914.1:p.Arg207Met
XM_011520607.2:c.1238G>T	XP_011518909.1:p.Arg413Met
XM_011520608.2:c.1214G>T	XP_011518910.1:p.Arg405Met
XM_011520609.2:c.977G>T	XP_011518911.1:p.Arg326Met
XM_011520611.2:c.977G>T	XP_011518913.1:p.Arg326Met
XM_011520612.2:c.620G>T	XP_011518914.1:p.Arg207Met
XM_017018990.1:c.1106G>T	XP_016874479.1:p.Arg369Met
XM_017018991.1:c.977G>T	XP_016874480.1:p.Arg326Met
NM_001987.5:c.1241G>T MANE Select	NP_001978.1:p.Arg414Met