Canonical Allele Identifier: CA1716165794

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70766035G= , CM000669.2:g.70766035G=	GRCh38
NC_000007.13:g.70231021G= , CM000669.1:g.70231021G=	GRCh37
NC_000007.12:g.69868957G=	NCBI36
NG_034133.1:g.1172117G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342771.10:c.1469-79G= MANE Select	ENSP00000344087.4:n.1469-79G=
ENST00000443672.2:c.-197-79G=	ENSP00000393548.2:n.-197-79G=
ENST00000644359.1:c.95-79G=	ENSP00000494561.1:n.95-79G=
ENST00000644506.1:c.95-79G=	ENSP00000496672.1:n.95-79G=
ENST00000644939.1:c.1466-79G=	ENSP00000496726.1:n.1466-79G=
ENST00000647140.1:c.313-79G=
ENST00000656200.1:c.95-79G=	ENSP00000499508.1:n.95-79G=
ENST00000342771.8:c.1469-79G=	ENSP00000344087.4:n.1469-79G=
ENST00000406775.6:c.1469-79G=	ENSP00000385263.2:n.1469-79G=
ENST00000443672.1:c.94-79G=
ENST00000481994.1:n.76-79G=
ENST00000611706.4:c.725-79G=	ENSP00000478134.1:n.725-79G=
ENST00000615871.4:c.725-79G=	ENSP00000479325.1:n.725-79G=
NM_001127231.2:c.1469-79G=	NP_001120703.1:n.1469-79G=
NM_015570.3:c.1469-79G=	NP_056385.1:n.1469-79G=
XM_005250257.1:c.95-79G=	XP_005250314.1:n.95-79G=
XM_011516010.1:c.1469-79G=	XP_011514312.1:n.1469-79G=
XM_011516011.1:c.1466-79G=	XP_011514313.1:n.1466-79G=
XM_011516012.1:c.1469-79G=	XP_011514314.1:n.1469-79G=
XM_011516013.1:c.1469-79G=	XP_011514315.1:n.1469-79G=
XM_011516014.1:c.1469-79G=	XP_011514316.1:n.1469-79G=
XM_011516015.1:c.1469-79G=	XP_011514317.1:n.1469-79G=
XM_011516016.1:c.1178-79G=	XP_011514318.1:n.1178-79G=
XM_011516017.1:c.995-79G=	XP_011514319.1:n.995-79G=
XM_011516018.1:c.968-79G=	XP_011514320.1:n.968-79G=
XM_005250257.2:c.95-79G=	XP_005250314.1:n.95-79G=
XM_011516010.2:c.1469-79G=	XP_011514312.1:n.1469-79G=
XM_011516011.2:c.1466-79G=	XP_011514313.1:n.1466-79G=
XM_011516012.2:c.1469-79G=	XP_011514314.1:n.1469-79G=
XM_011516013.2:c.1469-79G=	XP_011514315.1:n.1469-79G=
XM_011516014.2:c.1469-79G=	XP_011514316.1:n.1469-79G=
XM_011516017.2:c.995-79G=	XP_011514319.1:n.995-79G=
XM_011516018.2:c.968-79G=	XP_011514320.1:n.968-79G=
XM_017011951.2:c.1469-79G=	XP_016867440.1:n.1469-79G=
NM_001127231.3:c.1469-79G=	NP_001120703.1:n.1469-79G=
NM_015570.4:c.1469-79G= MANE Select	NP_056385.1:n.1469-79G=