Canonical Allele Identifier: CA1716160993

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70762954G= , CM000669.2:g.70762954G=	GRCh38
NC_000007.13:g.70227940G= , CM000669.1:g.70227940G=	GRCh37
NC_000007.12:g.69865876G=	NCBI36
NG_034133.1:g.1169036G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.827G= MANE Select	ENSP00000344087.4:p.Arg276=
ENST00000443672.2:c.-197-3160G=	ENSP00000393548.2:n.-197-3160G=
ENST00000644359.1:c.-545G=	ENSP00000494561.1:n.-545G=
ENST00000644506.1:c.-545G=	ENSP00000496672.1:n.-545G=
ENST00000644939.1:c.827G=	ENSP00000496726.1:p.Arg276=
ENST00000656200.1:c.-548G=	ENSP00000499508.1:n.-548G=
ENST00000342771.8:c.827G=	ENSP00000344087.4:p.Arg276=
ENST00000406775.6:c.827G=	ENSP00000385263.2:p.Arg276=
ENST00000416482.1:c.168G=
ENST00000611706.4:c.83G=	ENSP00000478134.1:p.Arg28=
ENST00000615871.4:c.83G=	ENSP00000479325.1:p.Arg28=
NM_001127231.2:c.827G=	NP_001120703.1:p.Arg276=
NM_015570.3:c.827G=	NP_056385.1:p.Arg276=
XM_011516010.1:c.827G=	XP_011514312.1:p.Arg276=
XM_011516011.1:c.827G=	XP_011514313.1:p.Arg276=
XM_011516012.1:c.827G=	XP_011514314.1:p.Arg276=
XM_011516013.1:c.827G=	XP_011514315.1:p.Arg276=
XM_011516014.1:c.827G=	XP_011514316.1:p.Arg276=
XM_011516015.1:c.827G=	XP_011514317.1:p.Arg276=
XM_011516016.1:c.536G=	XP_011514318.1:p.Arg179=
XM_011516017.1:c.353G=	XP_011514319.1:p.Arg118=
XM_011516018.1:c.326G=	XP_011514320.1:p.Arg109=
XM_011516010.2:c.827G=	XP_011514312.1:p.Arg276=
XM_011516011.2:c.827G=	XP_011514313.1:p.Arg276=
XM_011516012.2:c.827G=	XP_011514314.1:p.Arg276=
XM_011516013.2:c.827G=	XP_011514315.1:p.Arg276=
XM_011516014.2:c.827G=	XP_011514316.1:p.Arg276=
XM_011516017.2:c.353G=	XP_011514319.1:p.Arg118=
XM_011516018.2:c.326G=	XP_011514320.1:p.Arg109=
XM_017011951.2:c.827G=	XP_016867440.1:p.Arg276=
NM_001127231.3:c.827G=	NP_001120703.1:p.Arg276=
NM_015570.4:c.827G= MANE Select	NP_056385.1:p.Arg276=