Canonical Allele Identifier: CA6454099

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11752473T>C , CM000674.2:g.11752473T>C	GRCh38
NC_000012.11:g.11905407T>C , CM000674.1:g.11905407T>C	GRCh37
NC_000012.10:g.11796674T>C	NCBI36
NG_011443.1:g.107620T>C , LRG_609:g.107620T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.57T>C MANE Select	ENSP00000379658.3:p.Pro19=
ENST00000396373.8:c.57T>C	ENSP00000379658.3:p.Pro19=
ENST00000541426.1:n.241T>C
ENST00000544715.1:n.331T>C
NM_001987.4:c.57T>C , LRG_609t1:c.57T>C	NP_001978.1:p.Pro19=
XM_011520607.1:c.54T>C	XP_011518909.1:p.Pro18=
XM_011520608.1:c.30T>C	XP_011518910.1:p.Pro10=
XM_011520611.1:c.-101-86667T>C	XP_011518913.1:n.-101-86667T>C
XM_011520607.2:c.54T>C	XP_011518909.1:p.Pro18=
XM_011520608.2:c.30T>C	XP_011518910.1:p.Pro10=
XM_011520611.2:c.-101-86667T>C	XP_011518913.1:n.-101-86667T>C
XM_017018990.1:c.57T>C	XP_016874479.1:p.Pro19=
XM_017018991.1:c.-1604T>C	XP_016874480.1:n.-1604T>C
NM_001987.5:c.57T>C MANE Select	NP_001978.1:p.Pro19=