Canonical Allele Identifier: CA367668663

Gene: AUTS2

Linked Data

• MyVariant Identifiers: chr7:g.70231109T>C (hg19) ; chr7:g.70766123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70766123T>C , CM000669.2:g.70766123T>C	GRCh38
NC_000007.13:g.70231109T>C , CM000669.1:g.70231109T>C	GRCh37
NC_000007.12:g.69869045T>C	NCBI36
NG_034133.1:g.1172205T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.1478T>C MANE Select	ENSP00000344087.4:p.Ile493Thr
ENST00000443672.2:c.-188T>C	ENSP00000393548.2:n.-188T>C
ENST00000644359.1:c.104T>C	ENSP00000494561.1:p.Ile35Thr
ENST00000644506.1:c.104T>C	ENSP00000496672.1:p.Ile35Thr
ENST00000644939.1:c.1475T>C	ENSP00000496726.1:p.Ile492Thr
ENST00000647140.1:c.322T>C
ENST00000656200.1:c.104T>C	ENSP00000499508.1:p.Ile35Thr
ENST00000342771.8:c.1478T>C	ENSP00000344087.4:p.Ile493Thr
ENST00000406775.6:c.1478T>C	ENSP00000385263.2:p.Ile493Thr
ENST00000443672.1:c.103T>C
ENST00000481994.1:n.85T>C
ENST00000611706.4:c.734T>C	ENSP00000478134.1:p.Ile245Thr
ENST00000615871.4:c.734T>C	ENSP00000479325.1:p.Ile245Thr
NM_001127231.2:c.1478T>C	NP_001120703.1:p.Ile493Thr
NM_015570.3:c.1478T>C	NP_056385.1:p.Ile493Thr
XM_005250257.1:c.104T>C	XP_005250314.1:p.Ile35Thr
XM_011516010.1:c.1478T>C	XP_011514312.1:p.Ile493Thr
XM_011516011.1:c.1475T>C	XP_011514313.1:p.Ile492Thr
XM_011516012.1:c.1478T>C	XP_011514314.1:p.Ile493Thr
XM_011516013.1:c.1478T>C	XP_011514315.1:p.Ile493Thr
XM_011516014.1:c.1478T>C	XP_011514316.1:p.Ile493Thr
XM_011516015.1:c.1478T>C	XP_011514317.1:p.Ile493Thr
XM_011516016.1:c.1187T>C	XP_011514318.1:p.Ile396Thr
XM_011516017.1:c.1004T>C	XP_011514319.1:p.Ile335Thr
XM_011516018.1:c.977T>C	XP_011514320.1:p.Ile326Thr
XM_005250257.2:c.104T>C	XP_005250314.1:p.Ile35Thr
XM_011516010.2:c.1478T>C	XP_011514312.1:p.Ile493Thr
XM_011516011.2:c.1475T>C	XP_011514313.1:p.Ile492Thr
XM_011516012.2:c.1478T>C	XP_011514314.1:p.Ile493Thr
XM_011516013.2:c.1478T>C	XP_011514315.1:p.Ile493Thr
XM_011516014.2:c.1478T>C	XP_011514316.1:p.Ile493Thr
XM_011516017.2:c.1004T>C	XP_011514319.1:p.Ile335Thr
XM_011516018.2:c.977T>C	XP_011514320.1:p.Ile326Thr
XM_017011951.2:c.1478T>C	XP_016867440.1:p.Ile493Thr
NM_001127231.3:c.1478T>C	NP_001120703.1:p.Ile493Thr
NM_015570.4:c.1478T>C MANE Select	NP_056385.1:p.Ile493Thr