Canonical Allele Identifier: CA367668746

Gene: AUTS2

Linked Data

• MyVariant Identifiers: chr7:g.70231148A>C (hg19) ; chr7:g.70766162A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70766162A>C , CM000669.2:g.70766162A>C	GRCh38
NC_000007.13:g.70231148A>C , CM000669.1:g.70231148A>C	GRCh37
NC_000007.12:g.69869084A>C	NCBI36
NG_034133.1:g.1172244A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.1517A>C MANE Select	ENSP00000344087.4:p.Gln506Pro
ENST00000443672.2:c.-149A>C	ENSP00000393548.2:n.-149A>C
ENST00000644359.1:c.143A>C	ENSP00000494561.1:p.Gln48Pro
ENST00000644506.1:c.143A>C	ENSP00000496672.1:p.Gln48Pro
ENST00000644939.1:c.1514A>C	ENSP00000496726.1:p.Gln505Pro
ENST00000647140.1:c.361A>C
ENST00000656200.1:c.143A>C	ENSP00000499508.1:p.Gln48Pro
ENST00000342771.8:c.1517A>C	ENSP00000344087.4:p.Gln506Pro
ENST00000406775.6:c.1517A>C	ENSP00000385263.2:p.Gln506Pro
ENST00000443672.1:c.142A>C
ENST00000481994.1:n.124A>C
ENST00000611706.4:c.773A>C	ENSP00000478134.1:p.Gln258Pro
ENST00000615871.4:c.773A>C	ENSP00000479325.1:p.Gln258Pro
NM_001127231.2:c.1517A>C	NP_001120703.1:p.Gln506Pro
NM_015570.3:c.1517A>C	NP_056385.1:p.Gln506Pro
XM_005250257.1:c.143A>C	XP_005250314.1:p.Gln48Pro
XM_011516010.1:c.1517A>C	XP_011514312.1:p.Gln506Pro
XM_011516011.1:c.1514A>C	XP_011514313.1:p.Gln505Pro
XM_011516012.1:c.1517A>C	XP_011514314.1:p.Gln506Pro
XM_011516013.1:c.1517A>C	XP_011514315.1:p.Gln506Pro
XM_011516014.1:c.1517A>C	XP_011514316.1:p.Gln506Pro
XM_011516015.1:c.1517A>C	XP_011514317.1:p.Gln506Pro
XM_011516016.1:c.1226A>C	XP_011514318.1:p.Gln409Pro
XM_011516017.1:c.1043A>C	XP_011514319.1:p.Gln348Pro
XM_011516018.1:c.1016A>C	XP_011514320.1:p.Gln339Pro
XM_005250257.2:c.143A>C	XP_005250314.1:p.Gln48Pro
XM_011516010.2:c.1517A>C	XP_011514312.1:p.Gln506Pro
XM_011516011.2:c.1514A>C	XP_011514313.1:p.Gln505Pro
XM_011516012.2:c.1517A>C	XP_011514314.1:p.Gln506Pro
XM_011516013.2:c.1517A>C	XP_011514315.1:p.Gln506Pro
XM_011516014.2:c.1517A>C	XP_011514316.1:p.Gln506Pro
XM_011516017.2:c.1043A>C	XP_011514319.1:p.Gln348Pro
XM_011516018.2:c.1016A>C	XP_011514320.1:p.Gln339Pro
XM_017011951.2:c.1517A>C	XP_016867440.1:p.Gln506Pro
NM_001127231.3:c.1517A>C	NP_001120703.1:p.Gln506Pro
NM_015570.4:c.1517A>C MANE Select	NP_056385.1:p.Gln506Pro