Canonical Allele Identifier: CA2578902340

Gene: AUTS2

Linked Data

• gnomAD v4: 7-70777066-G-GTCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70777067_70777070dup , CM000669.2:g.70777067_70777070dup	GRCh38
NC_000007.13:g.70242053_70242056dup , CM000669.1:g.70242053_70242056dup	GRCh37
NC_000007.12:g.69879989_69879992dup	NCBI36
NG_034133.1:g.1183149_1183152dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000342771.10:c.1933-36_1933-33dup MANE Select	ENSP00000344087.4:n.1933-36_1933-33dup
ENST00000439256.2:c.31-36_31-33dup	ENSP00000407058.2:n.31-36_31-33dup
ENST00000443672.2:c.268-36_268-33dup	ENSP00000393548.2:n.268-36_268-33dup
ENST00000449547.6:c.26-36_26-33dup
ENST00000464768.2:n.601-36_601-33dup
ENST00000644359.1:c.514-36_514-33dup	ENSP00000494561.1:n.514-36_514-33dup
ENST00000644506.1:c.559-36_559-33dup	ENSP00000496672.1:n.559-36_559-33dup
ENST00000644939.1:c.1930-36_1930-33dup	ENSP00000496726.1:n.1930-36_1930-33dup
ENST00000644949.1:c.264-36_264-33dup
ENST00000646136.1:n.244-36_244-33dup
ENST00000647140.1:c.798-36_798-33dup
ENST00000342771.8:c.1933-36_1933-33dup	ENSP00000344087.4:n.1933-36_1933-33dup
ENST00000406775.6:c.1861-36_1861-33dup	ENSP00000385263.2:n.1861-36_1861-33dup
ENST00000439256.1:c.31-36_31-33dup
ENST00000443672.1:c.513-36_513-33dup
ENST00000464768.1:n.599-36_599-33dup
ENST00000465899.1:n.394_397dup
ENST00000498384.5:n.301-36_301-33dup
ENST00000611706.4:c.1189-36_1189-33dup	ENSP00000478134.1:n.1189-36_1189-33dup
ENST00000615871.4:c.1117-36_1117-33dup	ENSP00000479325.1:n.1117-36_1117-33dup
NM_001127231.2:c.1861-36_1861-33dup	NP_001120703.1:n.1861-36_1861-33dup
NM_015570.3:c.1933-36_1933-33dup	NP_056385.1:n.1933-36_1933-33dup
XM_005250257.1:c.580-36_580-33dup	XP_005250314.1:n.580-36_580-33dup
XM_011516010.1:c.1954-36_1954-33dup	XP_011514312.1:n.1954-36_1954-33dup
XM_011516011.1:c.1951-36_1951-33dup	XP_011514313.1:n.1951-36_1951-33dup
XM_011516012.1:c.1888-36_1888-33dup	XP_011514314.1:n.1888-36_1888-33dup
XM_011516013.1:c.1882-36_1882-33dup	XP_011514315.1:n.1882-36_1882-33dup
XM_011516014.1:c.1852-36_1852-33dup	XP_011514316.1:n.1852-36_1852-33dup
XM_011516015.1:c.1690-36_1690-33dup	XP_011514317.1:n.1690-36_1690-33dup
XM_011516016.1:c.1663-36_1663-33dup	XP_011514318.1:n.1663-36_1663-33dup
XM_011516017.1:c.1480-36_1480-33dup	XP_011514319.1:n.1480-36_1480-33dup
XM_011516018.1:c.1453-36_1453-33dup	XP_011514320.1:n.1453-36_1453-33dup
XM_005250257.2:c.580-36_580-33dup	XP_005250314.1:n.580-36_580-33dup
XM_011516010.2:c.1954-36_1954-33dup	XP_011514312.1:n.1954-36_1954-33dup
XM_011516011.2:c.1951-36_1951-33dup	XP_011514313.1:n.1951-36_1951-33dup
XM_011516012.2:c.1888-36_1888-33dup	XP_011514314.1:n.1888-36_1888-33dup
XM_011516013.2:c.1882-36_1882-33dup	XP_011514315.1:n.1882-36_1882-33dup
XM_011516014.2:c.1852-36_1852-33dup	XP_011514316.1:n.1852-36_1852-33dup
XM_011516017.2:c.1480-36_1480-33dup	XP_011514319.1:n.1480-36_1480-33dup
XM_011516018.2:c.1453-36_1453-33dup	XP_011514320.1:n.1453-36_1453-33dup
XM_017011951.2:c.1954-36_1954-33dup	XP_016867440.1:n.1954-36_1954-33dup
NM_001127231.3:c.1861-36_1861-33dup	NP_001120703.1:n.1861-36_1861-33dup
NM_015570.4:c.1933-36_1933-33dup MANE Select	NP_056385.1:n.1933-36_1933-33dup