Canonical Allele Identifier: CA13613739

Gene: ETV6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11702690A>C , CM000674.2:g.11702690A>C	GRCh38
NC_000012.11:g.11855624A>C , CM000674.1:g.11855624A>C	GRCh37
NC_000012.10:g.11746891A>C	NCBI36
NG_011443.1:g.57837A>C , LRG_609:g.57837A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.34-49760A>C MANE Select	ENSP00000379658.3:n.34-49760A>C
ENST00000396373.8:c.34-49760A>C	ENSP00000379658.3:n.34-49760A>C
ENST00000541426.1:n.218-49760A>C
ENST00000544715.1:n.151-13897A>C
NM_001987.4:c.34-49760A>C , LRG_609t1:c.34-49760A>C	NP_001978.1:n.34-49760A>C
XM_011520607.1:c.34-49763A>C	XP_011518909.1:n.34-49763A>C
XM_011520611.1:c.-102+52530A>C	XP_011518913.1:n.-102+52530A>C
XM_011520607.2:c.34-49763A>C	XP_011518909.1:n.34-49763A>C
XM_011520611.2:c.-102+52530A>C	XP_011518913.1:n.-102+52530A>C
XM_017018990.1:c.34-49760A>C	XP_016874479.1:n.34-49760A>C
XM_017018991.1:c.-1627-49760A>C	XP_016874480.1:n.-1627-49760A>C
NM_001987.5:c.34-49760A>C MANE Select	NP_001978.1:n.34-49760A>C