Canonical Allele Identifier: CA2776369923

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70777072_70777075del , CM000669.2:g.70777072_70777075del	GRCh38
NC_000007.13:g.70242058_70242061del , CM000669.1:g.70242058_70242061del	GRCh37
NC_000007.12:g.69879994_69879997del	NCBI36
NG_034133.1:g.1183154_1183157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.1933-31_1933-28del MANE Select	ENSP00000344087.4:n.1933-31_1933-28del
ENST00000439256.2:c.31-31_31-28del	ENSP00000407058.2:n.31-31_31-28del
ENST00000443672.2:c.268-31_268-28del	ENSP00000393548.2:n.268-31_268-28del
ENST00000449547.6:c.26-31_26-28del
ENST00000464768.2:n.601-31_601-28del
ENST00000644359.1:c.514-31_514-28del	ENSP00000494561.1:n.514-31_514-28del
ENST00000644506.1:c.559-31_559-28del	ENSP00000496672.1:n.559-31_559-28del
ENST00000644939.1:c.1930-31_1930-28del	ENSP00000496726.1:n.1930-31_1930-28del
ENST00000644949.1:c.264-31_264-28del
ENST00000646136.1:n.244-31_244-28del
ENST00000647140.1:c.798-31_798-28del
ENST00000342771.8:c.1933-31_1933-28del	ENSP00000344087.4:n.1933-31_1933-28del
ENST00000406775.6:c.1861-31_1861-28del	ENSP00000385263.2:n.1861-31_1861-28del
ENST00000439256.1:c.31-31_31-28del
ENST00000443672.1:c.513-31_513-28del
ENST00000464768.1:n.599-31_599-28del
ENST00000465899.1:n.399_402del
ENST00000498384.5:n.301-31_301-28del
ENST00000611706.4:c.1189-31_1189-28del	ENSP00000478134.1:n.1189-31_1189-28del
ENST00000615871.4:c.1117-31_1117-28del	ENSP00000479325.1:n.1117-31_1117-28del
NM_001127231.2:c.1861-31_1861-28del	NP_001120703.1:n.1861-31_1861-28del
NM_015570.3:c.1933-31_1933-28del	NP_056385.1:n.1933-31_1933-28del
XM_005250257.1:c.580-31_580-28del	XP_005250314.1:n.580-31_580-28del
XM_011516010.1:c.1954-31_1954-28del	XP_011514312.1:n.1954-31_1954-28del
XM_011516011.1:c.1951-31_1951-28del	XP_011514313.1:n.1951-31_1951-28del
XM_011516012.1:c.1888-31_1888-28del	XP_011514314.1:n.1888-31_1888-28del
XM_011516013.1:c.1882-31_1882-28del	XP_011514315.1:n.1882-31_1882-28del
XM_011516014.1:c.1852-31_1852-28del	XP_011514316.1:n.1852-31_1852-28del
XM_011516015.1:c.1690-31_1690-28del	XP_011514317.1:n.1690-31_1690-28del
XM_011516016.1:c.1663-31_1663-28del	XP_011514318.1:n.1663-31_1663-28del
XM_011516017.1:c.1480-31_1480-28del	XP_011514319.1:n.1480-31_1480-28del
XM_011516018.1:c.1453-31_1453-28del	XP_011514320.1:n.1453-31_1453-28del
XM_005250257.2:c.580-31_580-28del	XP_005250314.1:n.580-31_580-28del
XM_011516010.2:c.1954-31_1954-28del	XP_011514312.1:n.1954-31_1954-28del
XM_011516011.2:c.1951-31_1951-28del	XP_011514313.1:n.1951-31_1951-28del
XM_011516012.2:c.1888-31_1888-28del	XP_011514314.1:n.1888-31_1888-28del
XM_011516013.2:c.1882-31_1882-28del	XP_011514315.1:n.1882-31_1882-28del
XM_011516014.2:c.1852-31_1852-28del	XP_011514316.1:n.1852-31_1852-28del
XM_011516017.2:c.1480-31_1480-28del	XP_011514319.1:n.1480-31_1480-28del
XM_011516018.2:c.1453-31_1453-28del	XP_011514320.1:n.1453-31_1453-28del
XM_017011951.2:c.1954-31_1954-28del	XP_016867440.1:n.1954-31_1954-28del
NM_001127231.3:c.1861-31_1861-28del	NP_001120703.1:n.1861-31_1861-28del
NM_015570.4:c.1933-31_1933-28del MANE Select	NP_056385.1:n.1933-31_1933-28del