Canonical Allele Identifier: CA384044967

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038931G>T (hg19) ; chr12:g.11885997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885997G>T , CM000674.2:g.11885997G>T	GRCh38
NC_000012.11:g.12038931G>T , CM000674.1:g.12038931G>T	GRCh37
NC_000012.10:g.11930198G>T	NCBI36
NG_011443.1:g.241144G>T , LRG_609:g.241144G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1224G>T MANE Select	ENSP00000379658.3:p.Arg408Ser
ENST00000266427.3:c.61G>T
ENST00000396373.8:c.1224G>T	ENSP00000379658.3:p.Arg408Ser
NM_001987.4:c.1224G>T , LRG_609t1:c.1224G>T	NP_001978.1:p.Arg408Ser
XM_011520607.1:c.1221G>T	XP_011518909.1:p.Arg407Ser
XM_011520608.1:c.1197G>T	XP_011518910.1:p.Arg399Ser
XM_011520609.1:c.960G>T	XP_011518911.1:p.Arg320Ser
XM_011520610.1:c.960G>T	XP_011518912.1:p.Arg320Ser
XM_011520611.1:c.960G>T	XP_011518913.1:p.Arg320Ser
XM_011520612.1:c.603G>T	XP_011518914.1:p.Arg201Ser
XM_011520607.2:c.1221G>T	XP_011518909.1:p.Arg407Ser
XM_011520608.2:c.1197G>T	XP_011518910.1:p.Arg399Ser
XM_011520609.2:c.960G>T	XP_011518911.1:p.Arg320Ser
XM_011520611.2:c.960G>T	XP_011518913.1:p.Arg320Ser
XM_011520612.2:c.603G>T	XP_011518914.1:p.Arg201Ser
XM_017018990.1:c.1089G>T	XP_016874479.1:p.Arg363Ser
XM_017018991.1:c.960G>T	XP_016874480.1:p.Arg320Ser
NM_001987.5:c.1224G>T MANE Select	NP_001978.1:p.Arg408Ser