Canonical Allele Identifier: CA367668950

Gene: AUTS2

Linked Data

• MyVariant Identifiers: chr7:g.70231239G>T (hg19) ; chr7:g.70766253G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70766253G>T , CM000669.2:g.70766253G>T	GRCh38
NC_000007.13:g.70231239G>T , CM000669.1:g.70231239G>T	GRCh37
NC_000007.12:g.69869175G>T	NCBI36
NG_034133.1:g.1172335G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.1608G>T MANE Select	ENSP00000344087.4:p.Gln536His
ENST00000443672.2:c.-58G>T	ENSP00000393548.2:n.-58G>T
ENST00000644359.1:c.234G>T	ENSP00000494561.1:p.Gln78His
ENST00000644506.1:c.234G>T	ENSP00000496672.1:p.Gln78His
ENST00000644939.1:c.1605G>T	ENSP00000496726.1:p.Gln535His
ENST00000644949.1:c.20G>T
ENST00000647140.1:c.452G>T
ENST00000656200.1:c.234G>T	ENSP00000499508.1:p.Gln78His
ENST00000342771.8:c.1608G>T	ENSP00000344087.4:p.Gln536His
ENST00000406775.6:c.1608G>T	ENSP00000385263.2:p.Gln536His
ENST00000443672.1:c.233G>T
ENST00000481994.1:n.215G>T
ENST00000611706.4:c.864G>T	ENSP00000478134.1:p.Gln288His
ENST00000615871.4:c.864G>T	ENSP00000479325.1:p.Gln288His
NM_001127231.2:c.1608G>T	NP_001120703.1:p.Gln536His
NM_015570.3:c.1608G>T	NP_056385.1:p.Gln536His
XM_005250257.1:c.234G>T	XP_005250314.1:p.Gln78His
XM_011516010.1:c.1608G>T	XP_011514312.1:p.Gln536His
XM_011516011.1:c.1605G>T	XP_011514313.1:p.Gln535His
XM_011516012.1:c.1608G>T	XP_011514314.1:p.Gln536His
XM_011516013.1:c.1608G>T	XP_011514315.1:p.Gln536His
XM_011516014.1:c.1608G>T	XP_011514316.1:p.Gln536His
XM_011516015.1:c.1608G>T	XP_011514317.1:p.Gln536His
XM_011516016.1:c.1317G>T	XP_011514318.1:p.Gln439His
XM_011516017.1:c.1134G>T	XP_011514319.1:p.Gln378His
XM_011516018.1:c.1107G>T	XP_011514320.1:p.Gln369His
XM_005250257.2:c.234G>T	XP_005250314.1:p.Gln78His
XM_011516010.2:c.1608G>T	XP_011514312.1:p.Gln536His
XM_011516011.2:c.1605G>T	XP_011514313.1:p.Gln535His
XM_011516012.2:c.1608G>T	XP_011514314.1:p.Gln536His
XM_011516013.2:c.1608G>T	XP_011514315.1:p.Gln536His
XM_011516014.2:c.1608G>T	XP_011514316.1:p.Gln536His
XM_011516017.2:c.1134G>T	XP_011514319.1:p.Gln378His
XM_011516018.2:c.1107G>T	XP_011514320.1:p.Gln369His
XM_017011951.2:c.1608G>T	XP_016867440.1:p.Gln536His
NM_001127231.3:c.1608G>T	NP_001120703.1:p.Gln536His
NM_015570.4:c.1608G>T MANE Select	NP_056385.1:p.Gln536His