Canonical Allele Identifier: CA1716031900

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70580830_70580831delinsCT , CM000669.2:g.70580830_70580831delinsCT	GRCh38
NC_000007.13:g.70045816_70045817delinsCT , CM000669.1:g.70045816_70045817delinsCT	GRCh37
NC_000007.12:g.69683752_69683753delinsCT	NCBI36
NG_034133.1:g.986912_986913delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000342771.10:c.691-117739_691-117738delinsCT MANE Select	ENSP00000344087.4:n.691-117739_691-117738delinsCT
ENST00000644939.1:c.691-117739_691-117738delinsCT	ENSP00000496726.1:n.691-117739_691-117738delinsCT
ENST00000342771.8:c.691-117739_691-117738delinsCT	ENSP00000344087.4:n.691-117739_691-117738delinsCT
ENST00000406775.6:c.691-117739_691-117738delinsCT	ENSP00000385263.2:n.691-117739_691-117738delinsCT
NM_001127231.2:c.691-117739_691-117738delinsCT	NP_001120703.1:n.691-117739_691-117738delinsCT
NM_015570.3:c.691-117739_691-117738delinsCT	NP_056385.1:n.691-117739_691-117738delinsCT
XM_011516010.1:c.691-117739_691-117738delinsCT	XP_011514312.1:n.691-117739_691-117738delinsCT
XM_011516011.1:c.691-117739_691-117738delinsCT	XP_011514313.1:n.691-117739_691-117738delinsCT
XM_011516012.1:c.691-117739_691-117738delinsCT	XP_011514314.1:n.691-117739_691-117738delinsCT
XM_011516013.1:c.691-117739_691-117738delinsCT	XP_011514315.1:n.691-117739_691-117738delinsCT
XM_011516014.1:c.691-117739_691-117738delinsCT	XP_011514316.1:n.691-117739_691-117738delinsCT
XM_011516015.1:c.691-117739_691-117738delinsCT	XP_011514317.1:n.691-117739_691-117738delinsCT
XM_011516016.1:c.400-117739_400-117738delinsCT	XP_011514318.1:n.400-117739_400-117738delinsCT
XM_011516017.1:c.217-117739_217-117738delinsCT	XP_011514319.1:n.217-117739_217-117738delinsCT
XM_011516018.1:c.190-117739_190-117738delinsCT	XP_011514320.1:n.190-117739_190-117738delinsCT
XM_011516010.2:c.691-117739_691-117738delinsCT	XP_011514312.1:n.691-117739_691-117738delinsCT
XM_011516011.2:c.691-117739_691-117738delinsCT	XP_011514313.1:n.691-117739_691-117738delinsCT
XM_011516012.2:c.691-117739_691-117738delinsCT	XP_011514314.1:n.691-117739_691-117738delinsCT
XM_011516013.2:c.691-117739_691-117738delinsCT	XP_011514315.1:n.691-117739_691-117738delinsCT
XM_011516014.2:c.691-117739_691-117738delinsCT	XP_011514316.1:n.691-117739_691-117738delinsCT
XM_011516017.2:c.217-117739_217-117738delinsCT	XP_011514319.1:n.217-117739_217-117738delinsCT
XM_011516018.2:c.190-117739_190-117738delinsCT	XP_011514320.1:n.190-117739_190-117738delinsCT
XM_017011951.2:c.691-117739_691-117738delinsCT	XP_016867440.1:n.691-117739_691-117738delinsCT
NM_001127231.3:c.691-117739_691-117738delinsCT	NP_001120703.1:n.691-117739_691-117738delinsCT
NM_015570.4:c.691-117739_691-117738delinsCT MANE Select	NP_056385.1:n.691-117739_691-117738delinsCT