Canonical Allele Identifier: CA384045001

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038945A>T (hg19) ; chr12:g.11886011A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886011A>T , CM000674.2:g.11886011A>T	GRCh38
NC_000012.11:g.12038945A>T , CM000674.1:g.12038945A>T	GRCh37
NC_000012.10:g.11930212A>T	NCBI36
NG_011443.1:g.241158A>T , LRG_609:g.241158A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1238A>T MANE Select	ENSP00000379658.3:p.Gln413Leu
ENST00000266427.3:c.75A>T
ENST00000396373.8:c.1238A>T	ENSP00000379658.3:p.Gln413Leu
NM_001987.4:c.1238A>T , LRG_609t1:c.1238A>T	NP_001978.1:p.Gln413Leu
XM_011520607.1:c.1235A>T	XP_011518909.1:p.Gln412Leu
XM_011520608.1:c.1211A>T	XP_011518910.1:p.Gln404Leu
XM_011520609.1:c.974A>T	XP_011518911.1:p.Gln325Leu
XM_011520610.1:c.974A>T	XP_011518912.1:p.Gln325Leu
XM_011520611.1:c.974A>T	XP_011518913.1:p.Gln325Leu
XM_011520612.1:c.617A>T	XP_011518914.1:p.Gln206Leu
XM_011520607.2:c.1235A>T	XP_011518909.1:p.Gln412Leu
XM_011520608.2:c.1211A>T	XP_011518910.1:p.Gln404Leu
XM_011520609.2:c.974A>T	XP_011518911.1:p.Gln325Leu
XM_011520611.2:c.974A>T	XP_011518913.1:p.Gln325Leu
XM_011520612.2:c.617A>T	XP_011518914.1:p.Gln206Leu
XM_017018990.1:c.1103A>T	XP_016874479.1:p.Gln368Leu
XM_017018991.1:c.974A>T	XP_016874480.1:p.Gln325Leu
NM_001987.5:c.1238A>T MANE Select	NP_001978.1:p.Gln413Leu