Canonical Allele Identifier: CA230924846
Gene: ETS1 HGNC NCBI

Linked Data

dbSNP Id: rs1128334

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128459064C>T , CM000673.2:g.128459064C>T GRCh38
NC_000011.9:g.128328959C>T , CM000673.1:g.128328959C>T GRCh37
NC_000011.8:g.127834169C>T NCBI36
NG_029555.1:g.133495G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000319397.7:c.*3297G>A ENSP00000324578.5:n.*3297G>A
ENST00000392668.8:c.*3297G>A MANE Select ENSP00000376436.3:n.*3297G>A
ENST00000535549.5:c.*3297G>A ENSP00000441430.1:n.*3297G>A
NM_001143820.1:c.*3297G>A NP_001137292.1:n.*3297G>A
NM_001162422.1:c.*3297G>A NP_001155894.1:n.*3297G>A
NM_005238.3:c.*3297G>A NP_005229.1:n.*3297G>A
XM_011542649.1:c.*3297G>A XP_011540951.1:n.*3297G>A
XM_011542650.1:c.*3297G>A XP_011540952.1:n.*3297G>A
XM_011542651.1:c.*3297G>A XP_011540953.1:n.*3297G>A
XM_011542652.1:c.*3297G>A XP_011540954.1:n.*3297G>A
XR_948164.1:n.7784C>T
XR_948165.1:n.5035C>T
NM_001330451.1:c.*3297G>A NP_001317380.1:n.*3297G>A
XM_017017314.1:c.*3297G>A XP_016872803.1:n.*3297G>A
XM_017017317.1:c.*3297G>A XP_016872806.1:n.*3297G>A
NM_001143820.2:c.*3297G>A MANE Select NP_001137292.1:n.*3297G>A
NM_001330451.2:c.*3297G>A NP_001317380.1:n.*3297G>A
NM_005238.4:c.*3297G>A NP_005229.1:n.*3297G>A
NM_001162422.2:c.*3297G>A NP_001155894.1:n.*3297G>A