Canonical Allele Identifier: CA684251262

Gene: ETV6

Linked Data

• dbSNP Id: rs1225351556
• gnomAD v3: 12-11885746-T-TAAAGGGTGGGC
• gnomAD v4: 12-11885746-T-TAAAGGGTGGGC
• MyVariant Identifiers: chr12:g.12038680_12038681insAAAGGGTGGGC (hg19) ; chr12:g.11885746_11885747insAAAGGGTGGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885756_11885757insCAAAGGGTGGG , CM000674.2:g.11885756_11885757insCAAAGGGTGGG	GRCh38
NC_000012.11:g.12038690_12038691insCAAAGGGTGGG , CM000674.1:g.12038690_12038691insCAAAGGGTGGG	GRCh37
NC_000012.10:g.11929957_11929958insCAAAGGGTGGG	NCBI36
NG_011443.1:g.240903_240904insCAAAGGGTGGG , LRG_609:g.240903_240904insCAAAGGGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-170_1153-169insCAAAGGGTGGG MANE Select	ENSP00000379658.3:n.1153-170_1153-169insCAAAGGGTGGG
ENST00000396373.8:c.1153-170_1153-169insCAAAGGGTGGG	ENSP00000379658.3:n.1153-170_1153-169insCAAAGGGTGGG
NM_001987.4:c.1153-170_1153-169insCAAAGGGTGGG , LRG_609t1:c.1153-170_1153-169insCAAAGGGTGGG	NP_001978.1:n.1153-170_1153-169insCAAAGGGTGGG
XM_011520607.1:c.1150-170_1150-169insCAAAGGGTGGG	XP_011518909.1:n.1150-170_1150-169insCAAAGGGTGGG
XM_011520608.1:c.1126-170_1126-169insCAAAGGGTGGG	XP_011518910.1:n.1126-170_1126-169insCAAAGGGTGGG
XM_011520609.1:c.889-170_889-169insCAAAGGGTGGG	XP_011518911.1:n.889-170_889-169insCAAAGGGTGGG
XM_011520610.1:c.889-170_889-169insCAAAGGGTGGG	XP_011518912.1:n.889-170_889-169insCAAAGGGTGGG
XM_011520611.1:c.889-170_889-169insCAAAGGGTGGG	XP_011518913.1:n.889-170_889-169insCAAAGGGTGGG
XM_011520612.1:c.532-170_532-169insCAAAGGGTGGG	XP_011518914.1:n.532-170_532-169insCAAAGGGTGGG
XM_011520607.2:c.1150-170_1150-169insCAAAGGGTGGG	XP_011518909.1:n.1150-170_1150-169insCAAAGGGTGGG
XM_011520608.2:c.1126-170_1126-169insCAAAGGGTGGG	XP_011518910.1:n.1126-170_1126-169insCAAAGGGTGGG
XM_011520609.2:c.889-170_889-169insCAAAGGGTGGG	XP_011518911.1:n.889-170_889-169insCAAAGGGTGGG
XM_011520611.2:c.889-170_889-169insCAAAGGGTGGG	XP_011518913.1:n.889-170_889-169insCAAAGGGTGGG
XM_011520612.2:c.532-170_532-169insCAAAGGGTGGG	XP_011518914.1:n.532-170_532-169insCAAAGGGTGGG
XM_017018990.1:c.1018-170_1018-169insCAAAGGGTGGG	XP_016874479.1:n.1018-170_1018-169insCAAAGGGTGGG
XM_017018991.1:c.889-170_889-169insCAAAGGGTGGG	XP_016874480.1:n.889-170_889-169insCAAAGGGTGGG
NM_001987.5:c.1153-170_1153-169insCAAAGGGTGGG MANE Select	NP_001978.1:n.1153-170_1153-169insCAAAGGGTGGG