Canonical Allele Identifier: CA1716145453

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70777126G= , CM000669.2:g.70777126G=	GRCh38
NC_000007.13:g.70242112G= , CM000669.1:g.70242112G=	GRCh37
NC_000007.12:g.69880048G=	NCBI36
NG_034133.1:g.1183208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700075.1:c.24G=	ENSP00000514784.1:p.Met8=
ENST00000342771.10:c.1956G= MANE Select	ENSP00000344087.4:p.Met652=
ENST00000439256.2:c.54G=	ENSP00000407058.2:p.Met18=
ENST00000443672.2:c.291G=	ENSP00000393548.2:p.Met97=
ENST00000449547.6:c.49G=
ENST00000464768.2:n.624G=
ENST00000644359.1:c.537G=	ENSP00000494561.1:p.Met179=
ENST00000644506.1:c.582G=	ENSP00000496672.1:p.Met194=
ENST00000644939.1:c.1953G=	ENSP00000496726.1:p.Met651=
ENST00000644949.1:c.287G=
ENST00000646136.1:n.267G=
ENST00000647140.1:c.821G=
ENST00000342771.8:c.1956G=	ENSP00000344087.4:p.Met652=
ENST00000406775.6:c.1884G=	ENSP00000385263.2:p.Met628=
ENST00000439256.1:c.54G=
ENST00000443672.1:c.536G=
ENST00000464768.1:n.622G=
ENST00000465899.1:n.453G=
ENST00000498384.5:n.324G=
ENST00000611706.4:c.1212G=	ENSP00000478134.1:p.Met404=
ENST00000615871.4:c.1140G=	ENSP00000479325.1:p.Met380=
NM_001127231.2:c.1884G=	NP_001120703.1:p.Met628=
NM_015570.3:c.1956G=	NP_056385.1:p.Met652=
XM_005250257.1:c.603G=	XP_005250314.1:p.Met201=
XM_011516010.1:c.1977G=	XP_011514312.1:p.Met659=
XM_011516011.1:c.1974G=	XP_011514313.1:p.Met658=
XM_011516012.1:c.1911G=	XP_011514314.1:p.Met637=
XM_011516013.1:c.1905G=	XP_011514315.1:p.Met635=
XM_011516014.1:c.1875G=	XP_011514316.1:p.Met625=
XM_011516015.1:c.1713G=	XP_011514317.1:p.Met571=
XM_011516016.1:c.1686G=	XP_011514318.1:p.Met562=
XM_011516017.1:c.1503G=	XP_011514319.1:p.Met501=
XM_011516018.1:c.1476G=	XP_011514320.1:p.Met492=
XM_005250257.2:c.603G=	XP_005250314.1:p.Met201=
XM_011516010.2:c.1977G=	XP_011514312.1:p.Met659=
XM_011516011.2:c.1974G=	XP_011514313.1:p.Met658=
XM_011516012.2:c.1911G=	XP_011514314.1:p.Met637=
XM_011516013.2:c.1905G=	XP_011514315.1:p.Met635=
XM_011516014.2:c.1875G=	XP_011514316.1:p.Met625=
XM_011516017.2:c.1503G=	XP_011514319.1:p.Met501=
XM_011516018.2:c.1476G=	XP_011514320.1:p.Met492=
XM_017011951.2:c.1977G=	XP_016867440.1:p.Met659=
NM_001127231.3:c.1884G=	NP_001120703.1:p.Met628=
NM_015570.4:c.1956G= MANE Select	NP_056385.1:p.Met652=