Canonical Allele Identifier: CA384044872

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038889G>T (hg19) ; chr12:g.11885955G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885955G>T , CM000674.2:g.11885955G>T	GRCh38
NC_000012.11:g.12038889G>T , CM000674.1:g.12038889G>T	GRCh37
NC_000012.10:g.11930156G>T	NCBI36
NG_011443.1:g.241102G>T , LRG_609:g.241102G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1182G>T MANE Select	ENSP00000379658.3:p.Met394Ile
ENST00000266427.3:c.19G>T
ENST00000396373.8:c.1182G>T	ENSP00000379658.3:p.Met394Ile
NM_001987.4:c.1182G>T , LRG_609t1:c.1182G>T	NP_001978.1:p.Met394Ile
XM_011520607.1:c.1179G>T	XP_011518909.1:p.Met393Ile
XM_011520608.1:c.1155G>T	XP_011518910.1:p.Met385Ile
XM_011520609.1:c.918G>T	XP_011518911.1:p.Met306Ile
XM_011520610.1:c.918G>T	XP_011518912.1:p.Met306Ile
XM_011520611.1:c.918G>T	XP_011518913.1:p.Met306Ile
XM_011520612.1:c.561G>T	XP_011518914.1:p.Met187Ile
XM_011520607.2:c.1179G>T	XP_011518909.1:p.Met393Ile
XM_011520608.2:c.1155G>T	XP_011518910.1:p.Met385Ile
XM_011520609.2:c.918G>T	XP_011518911.1:p.Met306Ile
XM_011520611.2:c.918G>T	XP_011518913.1:p.Met306Ile
XM_011520612.2:c.561G>T	XP_011518914.1:p.Met187Ile
XM_017018990.1:c.1047G>T	XP_016874479.1:p.Met349Ile
XM_017018991.1:c.918G>T	XP_016874480.1:p.Met306Ile
NM_001987.5:c.1182G>T MANE Select	NP_001978.1:p.Met394Ile