Canonical Allele Identifier: CA2617675079

Gene: ETV6

Linked Data

• gnomAD v4: 12-11886037-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886042del , CM000674.2:g.11886042del	GRCh38
NC_000012.11:g.12038976del , CM000674.1:g.12038976del	GRCh37
NC_000012.10:g.11930243del	NCBI36
NG_011443.1:g.241189del , LRG_609:g.241189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1253+16del MANE Select	ENSP00000379658.3:n.1253+16del
ENST00000266427.3:c.90+16del
ENST00000396373.8:c.1253+16del	ENSP00000379658.3:n.1253+16del
NM_001987.4:c.1253+16del , LRG_609t1:c.1253+16del	NP_001978.1:n.1253+16del
XM_011520607.1:c.1250+16del	XP_011518909.1:n.1250+16del
XM_011520608.1:c.1226+16del	XP_011518910.1:n.1226+16del
XM_011520609.1:c.989+16del	XP_011518911.1:n.989+16del
XM_011520610.1:c.989+16del	XP_011518912.1:n.989+16del
XM_011520611.1:c.989+16del	XP_011518913.1:n.989+16del
XM_011520612.1:c.632+16del	XP_011518914.1:n.632+16del
XM_011520607.2:c.1250+16del	XP_011518909.1:n.1250+16del
XM_011520608.2:c.1226+16del	XP_011518910.1:n.1226+16del
XM_011520609.2:c.989+16del	XP_011518911.1:n.989+16del
XM_011520611.2:c.989+16del	XP_011518913.1:n.989+16del
XM_011520612.2:c.632+16del	XP_011518914.1:n.632+16del
XM_017018990.1:c.1118+16del	XP_016874479.1:n.1118+16del
XM_017018991.1:c.989+16del	XP_016874480.1:n.989+16del
NM_001987.5:c.1253+16del MANE Select	NP_001978.1:n.1253+16del