Canonical Allele Identifier: CA1716145466
Gene: AUTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70777135C= , CM000669.2:g.70777135C= GRCh38
NC_000007.13:g.70242121C= , CM000669.1:g.70242121C= GRCh37
NC_000007.12:g.69880057C= NCBI36
NG_034133.1:g.1183217C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700075.1:c.33C= ENSP00000514784.1:p.His11=
ENST00000342771.10:c.1965C= MANE Select ENSP00000344087.4:p.His655=
ENST00000439256.2:c.63C= ENSP00000407058.2:p.His21=
ENST00000443672.2:c.300C= ENSP00000393548.2:p.His100=
ENST00000449547.6:c.58C=
ENST00000464768.2:n.633C=
ENST00000644359.1:c.546C= ENSP00000494561.1:p.His182=
ENST00000644506.1:c.591C= ENSP00000496672.1:p.His197=
ENST00000644939.1:c.1962C= ENSP00000496726.1:p.His654=
ENST00000644949.1:c.296C=
ENST00000646136.1:n.276C=
ENST00000647140.1:c.830C=
ENST00000342771.8:c.1965C= ENSP00000344087.4:p.His655=
ENST00000406775.6:c.1893C= ENSP00000385263.2:p.His631=
ENST00000439256.1:c.63C=
ENST00000464768.1:n.631C=
ENST00000465899.1:n.462C=
ENST00000498384.5:n.333C=
ENST00000611706.4:c.1221C= ENSP00000478134.1:p.His407=
ENST00000615871.4:c.1149C= ENSP00000479325.1:p.His383=
NM_001127231.2:c.1893C= NP_001120703.1:p.His631=
NM_015570.3:c.1965C= NP_056385.1:p.His655=
XM_005250257.1:c.612C= XP_005250314.1:p.His204=
XM_011516010.1:c.1986C= XP_011514312.1:p.His662=
XM_011516011.1:c.1983C= XP_011514313.1:p.His661=
XM_011516012.1:c.1920C= XP_011514314.1:p.His640=
XM_011516013.1:c.1914C= XP_011514315.1:p.His638=
XM_011516014.1:c.1884C= XP_011514316.1:p.His628=
XM_011516015.1:c.1722C= XP_011514317.1:p.His574=
XM_011516016.1:c.1695C= XP_011514318.1:p.His565=
XM_011516017.1:c.1512C= XP_011514319.1:p.His504=
XM_011516018.1:c.1485C= XP_011514320.1:p.His495=
XM_005250257.2:c.612C= XP_005250314.1:p.His204=
XM_011516010.2:c.1986C= XP_011514312.1:p.His662=
XM_011516011.2:c.1983C= XP_011514313.1:p.His661=
XM_011516012.2:c.1920C= XP_011514314.1:p.His640=
XM_011516013.2:c.1914C= XP_011514315.1:p.His638=
XM_011516014.2:c.1884C= XP_011514316.1:p.His628=
XM_011516017.2:c.1512C= XP_011514319.1:p.His504=
XM_011516018.2:c.1485C= XP_011514320.1:p.His495=
XM_017011951.2:c.1986C= XP_016867440.1:p.His662=
NM_001127231.3:c.1893C= NP_001120703.1:p.His631=
NM_015570.4:c.1965C= MANE Select NP_056385.1:p.His655=