Canonical Allele Identifier: CA673179398

Gene: ETS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128511079C>A , CM000673.2:g.128511079C>A	GRCh38
NC_000011.9:g.128380974C>A , CM000673.1:g.128380974C>A	GRCh37
NC_000011.8:g.127886184C>A	NCBI36
NG_029555.1:g.81480G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319397.7:c.82+10834G>T	ENSP00000324578.5:n.82+10834G>T
ENST00000319397.6:c.82+10834G>T	ENSP00000324578.5:n.82+10834G>T
ENST00000392668.8:c.215-20503G>T MANE Select	ENSP00000376436.3:n.215-20503G>T
ENST00000526145.6:c.82+10834G>T	ENSP00000433500.1:n.82+10834G>T
ENST00000531611.5:c.82+10834G>T	ENSP00000435666.1:n.82+10834G>T
ENST00000535549.5:c.82+10834G>T	ENSP00000441430.1:n.82+10834G>T
NM_001143820.1:c.215-20503G>T	NP_001137292.1:n.215-20503G>T
NM_001162422.1:c.82+10834G>T	NP_001155894.1:n.82+10834G>T
NM_005238.3:c.82+10834G>T	NP_005229.1:n.82+10834G>T
XM_011542649.1:c.215-13405G>T	XP_011540951.1:n.215-13405G>T
XM_011542650.1:c.82+10834G>T	XP_011540952.1:n.82+10834G>T
XM_011542651.1:c.215-13405G>T	XP_011540953.1:n.215-13405G>T
XM_011542652.1:c.82+10834G>T	XP_011540954.1:n.82+10834G>T
NM_001330451.1:c.82+10834G>T	NP_001317380.1:n.82+10834G>T
XM_017017314.1:c.215-20503G>T	XP_016872803.1:n.215-20503G>T
XM_017017315.2:c.110-20503G>T	XP_016872804.1:n.110-20503G>T
XM_017017317.1:c.215-20503G>T	XP_016872806.1:n.215-20503G>T
NM_001143820.2:c.215-20503G>T MANE Select	NP_001137292.1:n.215-20503G>T
NM_001330451.2:c.82+10834G>T	NP_001317380.1:n.82+10834G>T
NM_005238.4:c.82+10834G>T	NP_005229.1:n.82+10834G>T
NM_001162422.2:c.82+10834G>T	NP_001155894.1:n.82+10834G>T