Canonical Allele Identifier: CA2016614773
Gene: ETV6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11809639T>G , CM000674.2:g.11809639T>G GRCh38
NC_000012.11:g.11962573T>G , CM000674.1:g.11962573T>G GRCh37
NC_000012.10:g.11853840T>G NCBI36
NG_011443.1:g.164786T>G , LRG_609:g.164786T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.164-29501T>G MANE Select ENSP00000379658.3:n.164-29501T>G
ENST00000396373.8:c.164-29501T>G ENSP00000379658.3:n.164-29501T>G
ENST00000541426.1:n.348-16005T>G
ENST00000545027.1:c.80-29501T>G ENSP00000441463.1:n.80-29501T>G
NM_001987.4:c.164-29501T>G , LRG_609t1:c.164-29501T>G NP_001978.1:n.164-29501T>G
XM_011520607.1:c.161-29501T>G XP_011518909.1:n.161-29501T>G
XM_011520608.1:c.137-29501T>G XP_011518910.1:n.137-29501T>G
XM_011520611.1:c.-101-29501T>G XP_011518913.1:n.-101-29501T>G
XM_011520607.2:c.161-29501T>G XP_011518909.1:n.161-29501T>G
XM_011520608.2:c.137-29501T>G XP_011518910.1:n.137-29501T>G
XM_011520611.2:c.-101-29501T>G XP_011518913.1:n.-101-29501T>G
XM_017018990.1:c.164-29501T>G XP_016874479.1:n.164-29501T>G
XM_017018991.1:c.-1497-16005T>G XP_016874480.1:n.-1497-16005T>G
NM_001987.5:c.164-29501T>G MANE Select NP_001978.1:n.164-29501T>G