Canonical Allele Identifier: CA1716015769

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70422044A= , CM000669.2:g.70422044A=	GRCh38
NC_000007.13:g.69887030A= , CM000669.1:g.69887030A=	GRCh37
NC_000007.12:g.69524966A=	NCBI36
NG_034133.1:g.828126A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342771.10:c.661-13708A= MANE Select	ENSP00000344087.4:n.661-13708A=
ENST00000475660.2:n.132-13708A=
ENST00000643060.1:n.17-13708A=
ENST00000644939.1:c.661-13708A=	ENSP00000496726.1:n.661-13708A=
ENST00000342771.8:c.661-13708A=	ENSP00000344087.4:n.661-13708A=
ENST00000406775.6:c.661-13708A=	ENSP00000385263.2:n.661-13708A=
ENST00000475660.1:n.132-13708A=
NM_001127231.2:c.661-13708A=	NP_001120703.1:n.661-13708A=
NM_015570.3:c.661-13708A=	NP_056385.1:n.661-13708A=
XM_011516010.1:c.661-13708A=	XP_011514312.1:n.661-13708A=
XM_011516011.1:c.661-13708A=	XP_011514313.1:n.661-13708A=
XM_011516012.1:c.661-13708A=	XP_011514314.1:n.661-13708A=
XM_011516013.1:c.661-13708A=	XP_011514315.1:n.661-13708A=
XM_011516014.1:c.661-13708A=	XP_011514316.1:n.661-13708A=
XM_011516015.1:c.661-13708A=	XP_011514317.1:n.661-13708A=
XM_011516016.1:c.370-13708A=	XP_011514318.1:n.370-13708A=
XM_011516017.1:c.187-13708A=	XP_011514319.1:n.187-13708A=
XM_011516018.1:c.160-13708A=	XP_011514320.1:n.160-13708A=
XM_011516010.2:c.661-13708A=	XP_011514312.1:n.661-13708A=
XM_011516011.2:c.661-13708A=	XP_011514313.1:n.661-13708A=
XM_011516012.2:c.661-13708A=	XP_011514314.1:n.661-13708A=
XM_011516013.2:c.661-13708A=	XP_011514315.1:n.661-13708A=
XM_011516014.2:c.661-13708A=	XP_011514316.1:n.661-13708A=
XM_011516017.2:c.187-13708A=	XP_011514319.1:n.187-13708A=
XM_011516018.2:c.160-13708A=	XP_011514320.1:n.160-13708A=
XM_017011951.2:c.661-13708A=	XP_016867440.1:n.661-13708A=
NM_001127231.3:c.661-13708A=	NP_001120703.1:n.661-13708A=
NM_015570.4:c.661-13708A= MANE Select	NP_056385.1:n.661-13708A=