Canonical Allele Identifier: CA1716031954

Gene: AUTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70580948_70580949delinsCA , CM000669.2:g.70580948_70580949delinsCA	GRCh38
NC_000007.13:g.70045934_70045935delinsCA , CM000669.1:g.70045934_70045935delinsCA	GRCh37
NC_000007.12:g.69683870_69683871delinsCA	NCBI36
NG_034133.1:g.987030_987031delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.691-117621_691-117620delinsCA MANE Select	ENSP00000344087.4:n.691-117621_691-117620delinsCA
ENST00000644939.1:c.691-117621_691-117620delinsCA	ENSP00000496726.1:n.691-117621_691-117620delinsCA
ENST00000342771.8:c.691-117621_691-117620delinsCA	ENSP00000344087.4:n.691-117621_691-117620delinsCA
ENST00000406775.6:c.691-117621_691-117620delinsCA	ENSP00000385263.2:n.691-117621_691-117620delinsCA
NM_001127231.2:c.691-117621_691-117620delinsCA	NP_001120703.1:n.691-117621_691-117620delinsCA
NM_015570.3:c.691-117621_691-117620delinsCA	NP_056385.1:n.691-117621_691-117620delinsCA
XM_011516010.1:c.691-117621_691-117620delinsCA	XP_011514312.1:n.691-117621_691-117620delinsCA
XM_011516011.1:c.691-117621_691-117620delinsCA	XP_011514313.1:n.691-117621_691-117620delinsCA
XM_011516012.1:c.691-117621_691-117620delinsCA	XP_011514314.1:n.691-117621_691-117620delinsCA
XM_011516013.1:c.691-117621_691-117620delinsCA	XP_011514315.1:n.691-117621_691-117620delinsCA
XM_011516014.1:c.691-117621_691-117620delinsCA	XP_011514316.1:n.691-117621_691-117620delinsCA
XM_011516015.1:c.691-117621_691-117620delinsCA	XP_011514317.1:n.691-117621_691-117620delinsCA
XM_011516016.1:c.400-117621_400-117620delinsCA	XP_011514318.1:n.400-117621_400-117620delinsCA
XM_011516017.1:c.217-117621_217-117620delinsCA	XP_011514319.1:n.217-117621_217-117620delinsCA
XM_011516018.1:c.190-117621_190-117620delinsCA	XP_011514320.1:n.190-117621_190-117620delinsCA
XM_011516010.2:c.691-117621_691-117620delinsCA	XP_011514312.1:n.691-117621_691-117620delinsCA
XM_011516011.2:c.691-117621_691-117620delinsCA	XP_011514313.1:n.691-117621_691-117620delinsCA
XM_011516012.2:c.691-117621_691-117620delinsCA	XP_011514314.1:n.691-117621_691-117620delinsCA
XM_011516013.2:c.691-117621_691-117620delinsCA	XP_011514315.1:n.691-117621_691-117620delinsCA
XM_011516014.2:c.691-117621_691-117620delinsCA	XP_011514316.1:n.691-117621_691-117620delinsCA
XM_011516017.2:c.217-117621_217-117620delinsCA	XP_011514319.1:n.217-117621_217-117620delinsCA
XM_011516018.2:c.190-117621_190-117620delinsCA	XP_011514320.1:n.190-117621_190-117620delinsCA
XM_017011951.2:c.691-117621_691-117620delinsCA	XP_016867440.1:n.691-117621_691-117620delinsCA
NM_001127231.3:c.691-117621_691-117620delinsCA	NP_001120703.1:n.691-117621_691-117620delinsCA
NM_015570.4:c.691-117621_691-117620delinsCA MANE Select	NP_056385.1:n.691-117621_691-117620delinsCA