Canonical Allele Identifier: CA2683160677

Gene: AUTS2

Linked Data

• gnomAD v4: 7-70765965-C-CATTG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70765970_70765973dup , CM000669.2:g.70765970_70765973dup	GRCh38
NC_000007.13:g.70230956_70230959dup , CM000669.1:g.70230956_70230959dup	GRCh37
NC_000007.12:g.69868892_69868895dup	NCBI36
NG_034133.1:g.1172052_1172055dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000342771.10:c.1469-144_1469-141dup MANE Select	ENSP00000344087.4:n.1469-144_1469-141dup
ENST00000443672.2:c.-197-144_-197-141dup	ENSP00000393548.2:n.-197-144_-197-141dup
ENST00000644359.1:c.95-144_95-141dup	ENSP00000494561.1:n.95-144_95-141dup
ENST00000644506.1:c.95-144_95-141dup	ENSP00000496672.1:n.95-144_95-141dup
ENST00000644939.1:c.1466-144_1466-141dup	ENSP00000496726.1:n.1466-144_1466-141dup
ENST00000647140.1:c.313-144_313-141dup
ENST00000656200.1:c.95-144_95-141dup	ENSP00000499508.1:n.95-144_95-141dup
ENST00000342771.8:c.1469-144_1469-141dup	ENSP00000344087.4:n.1469-144_1469-141dup
ENST00000406775.6:c.1469-144_1469-141dup	ENSP00000385263.2:n.1469-144_1469-141dup
ENST00000443672.1:c.94-144_94-141dup
ENST00000481994.1:n.76-144_76-141dup
ENST00000611706.4:c.725-144_725-141dup	ENSP00000478134.1:n.725-144_725-141dup
ENST00000615871.4:c.725-144_725-141dup	ENSP00000479325.1:n.725-144_725-141dup
NM_001127231.2:c.1469-144_1469-141dup	NP_001120703.1:n.1469-144_1469-141dup
NM_015570.3:c.1469-144_1469-141dup	NP_056385.1:n.1469-144_1469-141dup
XM_005250257.1:c.95-144_95-141dup	XP_005250314.1:n.95-144_95-141dup
XM_011516010.1:c.1469-144_1469-141dup	XP_011514312.1:n.1469-144_1469-141dup
XM_011516011.1:c.1466-144_1466-141dup	XP_011514313.1:n.1466-144_1466-141dup
XM_011516012.1:c.1469-144_1469-141dup	XP_011514314.1:n.1469-144_1469-141dup
XM_011516013.1:c.1469-144_1469-141dup	XP_011514315.1:n.1469-144_1469-141dup
XM_011516014.1:c.1469-144_1469-141dup	XP_011514316.1:n.1469-144_1469-141dup
XM_011516015.1:c.1469-144_1469-141dup	XP_011514317.1:n.1469-144_1469-141dup
XM_011516016.1:c.1178-144_1178-141dup	XP_011514318.1:n.1178-144_1178-141dup
XM_011516017.1:c.995-144_995-141dup	XP_011514319.1:n.995-144_995-141dup
XM_011516018.1:c.968-144_968-141dup	XP_011514320.1:n.968-144_968-141dup
XM_005250257.2:c.95-144_95-141dup	XP_005250314.1:n.95-144_95-141dup
XM_011516010.2:c.1469-144_1469-141dup	XP_011514312.1:n.1469-144_1469-141dup
XM_011516011.2:c.1466-144_1466-141dup	XP_011514313.1:n.1466-144_1466-141dup
XM_011516012.2:c.1469-144_1469-141dup	XP_011514314.1:n.1469-144_1469-141dup
XM_011516013.2:c.1469-144_1469-141dup	XP_011514315.1:n.1469-144_1469-141dup
XM_011516014.2:c.1469-144_1469-141dup	XP_011514316.1:n.1469-144_1469-141dup
XM_011516017.2:c.995-144_995-141dup	XP_011514319.1:n.995-144_995-141dup
XM_011516018.2:c.968-144_968-141dup	XP_011514320.1:n.968-144_968-141dup
XM_017011951.2:c.1469-144_1469-141dup	XP_016867440.1:n.1469-144_1469-141dup
NM_001127231.3:c.1469-144_1469-141dup	NP_001120703.1:n.1469-144_1469-141dup
NM_015570.4:c.1469-144_1469-141dup MANE Select	NP_056385.1:n.1469-144_1469-141dup