Canonical Allele Identifier: CA367668945

Gene: AUTS2

Linked Data

• MyVariant Identifiers: chr7:g.70231237C>G (hg19) ; chr7:g.70766251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70766251C>G , CM000669.2:g.70766251C>G	GRCh38
NC_000007.13:g.70231237C>G , CM000669.1:g.70231237C>G	GRCh37
NC_000007.12:g.69869173C>G	NCBI36
NG_034133.1:g.1172333C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.1606C>G MANE Select	ENSP00000344087.4:p.Gln536Glu
ENST00000443672.2:c.-60C>G	ENSP00000393548.2:n.-60C>G
ENST00000644359.1:c.232C>G	ENSP00000494561.1:p.Gln78Glu
ENST00000644506.1:c.232C>G	ENSP00000496672.1:p.Gln78Glu
ENST00000644939.1:c.1603C>G	ENSP00000496726.1:p.Gln535Glu
ENST00000644949.1:c.18C>G
ENST00000647140.1:c.450C>G
ENST00000656200.1:c.232C>G	ENSP00000499508.1:p.Gln78Glu
ENST00000342771.8:c.1606C>G	ENSP00000344087.4:p.Gln536Glu
ENST00000406775.6:c.1606C>G	ENSP00000385263.2:p.Gln536Glu
ENST00000443672.1:c.231C>G
ENST00000481994.1:n.213C>G
ENST00000611706.4:c.862C>G	ENSP00000478134.1:p.Gln288Glu
ENST00000615871.4:c.862C>G	ENSP00000479325.1:p.Gln288Glu
NM_001127231.2:c.1606C>G	NP_001120703.1:p.Gln536Glu
NM_015570.3:c.1606C>G	NP_056385.1:p.Gln536Glu
XM_005250257.1:c.232C>G	XP_005250314.1:p.Gln78Glu
XM_011516010.1:c.1606C>G	XP_011514312.1:p.Gln536Glu
XM_011516011.1:c.1603C>G	XP_011514313.1:p.Gln535Glu
XM_011516012.1:c.1606C>G	XP_011514314.1:p.Gln536Glu
XM_011516013.1:c.1606C>G	XP_011514315.1:p.Gln536Glu
XM_011516014.1:c.1606C>G	XP_011514316.1:p.Gln536Glu
XM_011516015.1:c.1606C>G	XP_011514317.1:p.Gln536Glu
XM_011516016.1:c.1315C>G	XP_011514318.1:p.Gln439Glu
XM_011516017.1:c.1132C>G	XP_011514319.1:p.Gln378Glu
XM_011516018.1:c.1105C>G	XP_011514320.1:p.Gln369Glu
XM_005250257.2:c.232C>G	XP_005250314.1:p.Gln78Glu
XM_011516010.2:c.1606C>G	XP_011514312.1:p.Gln536Glu
XM_011516011.2:c.1603C>G	XP_011514313.1:p.Gln535Glu
XM_011516012.2:c.1606C>G	XP_011514314.1:p.Gln536Glu
XM_011516013.2:c.1606C>G	XP_011514315.1:p.Gln536Glu
XM_011516014.2:c.1606C>G	XP_011514316.1:p.Gln536Glu
XM_011516017.2:c.1132C>G	XP_011514319.1:p.Gln378Glu
XM_011516018.2:c.1105C>G	XP_011514320.1:p.Gln369Glu
XM_017011951.2:c.1606C>G	XP_016867440.1:p.Gln536Glu
NM_001127231.3:c.1606C>G	NP_001120703.1:p.Gln536Glu
NM_015570.4:c.1606C>G MANE Select	NP_056385.1:p.Gln536Glu