Canonical Allele Identifier: CA1716145477
Gene: AUTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70777138C= , CM000669.2:g.70777138C= GRCh38
NC_000007.13:g.70242124C= , CM000669.1:g.70242124C= GRCh37
NC_000007.12:g.69880060C= NCBI36
NG_034133.1:g.1183220C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700075.1:c.36C= ENSP00000514784.1:p.Ile12=
ENST00000342771.10:c.1968C= MANE Select ENSP00000344087.4:p.Ile656=
ENST00000439256.2:c.66C= ENSP00000407058.2:p.Ile22=
ENST00000443672.2:c.303C= ENSP00000393548.2:p.Ile101=
ENST00000449547.6:c.61C=
ENST00000464768.2:n.636C=
ENST00000644359.1:c.549C= ENSP00000494561.1:p.Ile183=
ENST00000644506.1:c.594C= ENSP00000496672.1:p.Ile198=
ENST00000644939.1:c.1965C= ENSP00000496726.1:p.Ile655=
ENST00000646136.1:n.279C=
ENST00000647140.1:c.833C=
ENST00000342771.8:c.1968C= ENSP00000344087.4:p.Ile656=
ENST00000406775.6:c.1896C= ENSP00000385263.2:p.Ile632=
ENST00000439256.1:c.66C=
ENST00000464768.1:n.634C=
ENST00000465899.1:n.465C=
ENST00000498384.5:n.336C=
ENST00000611706.4:c.1224C= ENSP00000478134.1:p.Ile408=
ENST00000615871.4:c.1152C= ENSP00000479325.1:p.Ile384=
NM_001127231.2:c.1896C= NP_001120703.1:p.Ile632=
NM_015570.3:c.1968C= NP_056385.1:p.Ile656=
XM_005250257.1:c.615C= XP_005250314.1:p.Ile205=
XM_011516010.1:c.1989C= XP_011514312.1:p.Ile663=
XM_011516011.1:c.1986C= XP_011514313.1:p.Ile662=
XM_011516012.1:c.1923C= XP_011514314.1:p.Ile641=
XM_011516013.1:c.1917C= XP_011514315.1:p.Ile639=
XM_011516014.1:c.1887C= XP_011514316.1:p.Ile629=
XM_011516015.1:c.1725C= XP_011514317.1:p.Ile575=
XM_011516016.1:c.1698C= XP_011514318.1:p.Ile566=
XM_011516017.1:c.1515C= XP_011514319.1:p.Ile505=
XM_011516018.1:c.1488C= XP_011514320.1:p.Ile496=
XM_005250257.2:c.615C= XP_005250314.1:p.Ile205=
XM_011516010.2:c.1989C= XP_011514312.1:p.Ile663=
XM_011516011.2:c.1986C= XP_011514313.1:p.Ile662=
XM_011516012.2:c.1923C= XP_011514314.1:p.Ile641=
XM_011516013.2:c.1917C= XP_011514315.1:p.Ile639=
XM_011516014.2:c.1887C= XP_011514316.1:p.Ile629=
XM_011516017.2:c.1515C= XP_011514319.1:p.Ile505=
XM_011516018.2:c.1488C= XP_011514320.1:p.Ile496=
XM_017011951.2:c.1989C= XP_016867440.1:p.Ile663=
NM_001127231.3:c.1896C= NP_001120703.1:p.Ile632=
NM_015570.4:c.1968C= MANE Select NP_056385.1:p.Ile656=