Canonical Allele Identifier: CA1716145542
Gene: AUTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70777169G= , CM000669.2:g.70777169G= GRCh38
NC_000007.13:g.70242155G= , CM000669.1:g.70242155G= GRCh37
NC_000007.12:g.69880091G= NCBI36
NG_034133.1:g.1183251G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700075.1:c.67G= ENSP00000514784.1:p.Val23=
ENST00000342771.10:c.1999G= MANE Select ENSP00000344087.4:p.Val667=
ENST00000439256.2:c.97G= ENSP00000407058.2:p.Val33=
ENST00000443672.2:c.334G= ENSP00000393548.2:p.Val112=
ENST00000449547.6:c.92G=
ENST00000464768.2:n.667G=
ENST00000644359.1:c.580G= ENSP00000494561.1:p.Val194=
ENST00000644506.1:c.625G= ENSP00000496672.1:p.Val209=
ENST00000644939.1:c.1996G= ENSP00000496726.1:p.Val666=
ENST00000646136.1:n.310G=
ENST00000647140.1:c.864G=
ENST00000342771.8:c.1999G= ENSP00000344087.4:p.Val667=
ENST00000406775.6:c.1927G= ENSP00000385263.2:p.Val643=
ENST00000439256.1:c.97G=
ENST00000464768.1:n.665G=
ENST00000465899.1:n.496G=
ENST00000498384.5:n.367G=
ENST00000611706.4:c.1255G= ENSP00000478134.1:p.Val419=
ENST00000615871.4:c.1183G= ENSP00000479325.1:p.Val395=
NM_001127231.2:c.1927G= NP_001120703.1:p.Val643=
NM_015570.3:c.1999G= NP_056385.1:p.Val667=
XM_005250257.1:c.646G= XP_005250314.1:p.Val216=
XM_011516010.1:c.2020G= XP_011514312.1:p.Val674=
XM_011516011.1:c.2017G= XP_011514313.1:p.Val673=
XM_011516012.1:c.1954G= XP_011514314.1:p.Val652=
XM_011516013.1:c.1948G= XP_011514315.1:p.Val650=
XM_011516014.1:c.1918G= XP_011514316.1:p.Val640=
XM_011516015.1:c.1756G= XP_011514317.1:p.Val586=
XM_011516016.1:c.1729G= XP_011514318.1:p.Val577=
XM_011516017.1:c.1546G= XP_011514319.1:p.Val516=
XM_011516018.1:c.1519G= XP_011514320.1:p.Val507=
XM_005250257.2:c.646G= XP_005250314.1:p.Val216=
XM_011516010.2:c.2020G= XP_011514312.1:p.Val674=
XM_011516011.2:c.2017G= XP_011514313.1:p.Val673=
XM_011516012.2:c.1954G= XP_011514314.1:p.Val652=
XM_011516013.2:c.1948G= XP_011514315.1:p.Val650=
XM_011516014.2:c.1918G= XP_011514316.1:p.Val640=
XM_011516017.2:c.1546G= XP_011514319.1:p.Val516=
XM_011516018.2:c.1519G= XP_011514320.1:p.Val507=
XM_017011951.2:c.2020G= XP_016867440.1:p.Val674=
NM_001127231.3:c.1927G= NP_001120703.1:p.Val643=
NM_015570.4:c.1999G= MANE Select NP_056385.1:p.Val667=