Canonical Allele Identifier: CA1716161159

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70763041C= , CM000669.2:g.70763041C=	GRCh38
NC_000007.13:g.70228027C= , CM000669.1:g.70228027C=	GRCh37
NC_000007.12:g.69865963C=	NCBI36
NG_034133.1:g.1169123C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342771.10:c.914C= MANE Select	ENSP00000344087.4:p.Pro305=
ENST00000443672.2:c.-197-3073C=	ENSP00000393548.2:n.-197-3073C=
ENST00000644359.1:c.-458C=	ENSP00000494561.1:n.-458C=
ENST00000644506.1:c.-458C=	ENSP00000496672.1:n.-458C=
ENST00000644939.1:c.914C=	ENSP00000496726.1:p.Pro305=
ENST00000656200.1:c.-461C=	ENSP00000499508.1:n.-461C=
ENST00000342771.8:c.914C=	ENSP00000344087.4:p.Pro305=
ENST00000406775.6:c.914C=	ENSP00000385263.2:p.Pro305=
ENST00000416482.1:c.255C=
ENST00000611706.4:c.170C=	ENSP00000478134.1:p.Pro57=
ENST00000615871.4:c.170C=	ENSP00000479325.1:p.Pro57=
NM_001127231.2:c.914C=	NP_001120703.1:p.Pro305=
NM_015570.3:c.914C=	NP_056385.1:p.Pro305=
XM_011516010.1:c.914C=	XP_011514312.1:p.Pro305=
XM_011516011.1:c.914C=	XP_011514313.1:p.Pro305=
XM_011516012.1:c.914C=	XP_011514314.1:p.Pro305=
XM_011516013.1:c.914C=	XP_011514315.1:p.Pro305=
XM_011516014.1:c.914C=	XP_011514316.1:p.Pro305=
XM_011516015.1:c.914C=	XP_011514317.1:p.Pro305=
XM_011516016.1:c.623C=	XP_011514318.1:p.Pro208=
XM_011516017.1:c.440C=	XP_011514319.1:p.Pro147=
XM_011516018.1:c.413C=	XP_011514320.1:p.Pro138=
XM_011516010.2:c.914C=	XP_011514312.1:p.Pro305=
XM_011516011.2:c.914C=	XP_011514313.1:p.Pro305=
XM_011516012.2:c.914C=	XP_011514314.1:p.Pro305=
XM_011516013.2:c.914C=	XP_011514315.1:p.Pro305=
XM_011516014.2:c.914C=	XP_011514316.1:p.Pro305=
XM_011516017.2:c.440C=	XP_011514319.1:p.Pro147=
XM_011516018.2:c.413C=	XP_011514320.1:p.Pro138=
XM_017011951.2:c.914C=	XP_016867440.1:p.Pro305=
NM_001127231.3:c.914C=	NP_001120703.1:p.Pro305=
NM_015570.4:c.914C= MANE Select	NP_056385.1:p.Pro305=