Canonical Allele Identifier: CA1716165782
Gene: AUTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70766030_70766039delinsGCCCCGTACC , CM000669.2:g.70766030_70766039delinsGCCCCGTACC GRCh38
NC_000007.13:g.70231016_70231025delinsGCCCCGTACC , CM000669.1:g.70231016_70231025delinsGCCCCGTACC GRCh37
NC_000007.12:g.69868952_69868961delinsGCCCCGTACC NCBI36
NG_034133.1:g.1172112_1172121delinsGCCCCGTACC

Transcript Alleles

HGVS Amino-acid change
ENST00000342771.10:c.1469-84_1469-75delinsGCCCCGTACC MANE Select ENSP00000344087.4:n.1469-84_1469-75delins...
ENST00000443672.2:c.-197-84_-197-75delinsGCCCCGTACC ENSP00000393548.2:n.-197-84_-197-75delins...
ENST00000644359.1:c.95-84_95-75delinsGCCCCGTACC ENSP00000494561.1:n.95-84_95-75delinsGCCC...
ENST00000644506.1:c.95-84_95-75delinsGCCCCGTACC ENSP00000496672.1:n.95-84_95-75delinsGCCC...
ENST00000644939.1:c.1466-84_1466-75delinsGCCCCGTACC ENSP00000496726.1:n.1466-84_1466-75delins...
ENST00000647140.1:c.313-84_313-75delinsGCCCCGTACC
ENST00000656200.1:c.95-84_95-75delinsGCCCCGTACC ENSP00000499508.1:n.95-84_95-75delinsGCCC...
ENST00000342771.8:c.1469-84_1469-75delinsGCCCCGTACC ENSP00000344087.4:n.1469-84_1469-75delins...
ENST00000406775.6:c.1469-84_1469-75delinsGCCCCGTACC ENSP00000385263.2:n.1469-84_1469-75delins...
ENST00000443672.1:c.94-84_94-75delinsGCCCCGTACC
ENST00000481994.1:n.76-84_76-75delinsGCCCCGTACC
ENST00000611706.4:c.725-84_725-75delinsGCCCCGTACC ENSP00000478134.1:n.725-84_725-75delinsGC...
ENST00000615871.4:c.725-84_725-75delinsGCCCCGTACC ENSP00000479325.1:n.725-84_725-75delinsGC...
NM_001127231.2:c.1469-84_1469-75delinsGCCCCGTACC NP_001120703.1:n.1469-84_1469-75delinsGCC...
NM_015570.3:c.1469-84_1469-75delinsGCCCCGTACC NP_056385.1:n.1469-84_1469-75delinsGCCCCG...
XM_005250257.1:c.95-84_95-75delinsGCCCCGTACC XP_005250314.1:n.95-84_95-75delinsGCCCCGT...
XM_011516010.1:c.1469-84_1469-75delinsGCCCCGTACC XP_011514312.1:n.1469-84_1469-75delinsGCC...
XM_011516011.1:c.1466-84_1466-75delinsGCCCCGTACC XP_011514313.1:n.1466-84_1466-75delinsGCC...
XM_011516012.1:c.1469-84_1469-75delinsGCCCCGTACC XP_011514314.1:n.1469-84_1469-75delinsGCC...
XM_011516013.1:c.1469-84_1469-75delinsGCCCCGTACC XP_011514315.1:n.1469-84_1469-75delinsGCC...
XM_011516014.1:c.1469-84_1469-75delinsGCCCCGTACC XP_011514316.1:n.1469-84_1469-75delinsGCC...
XM_011516015.1:c.1469-84_1469-75delinsGCCCCGTACC XP_011514317.1:n.1469-84_1469-75delinsGCC...
XM_011516016.1:c.1178-84_1178-75delinsGCCCCGTACC XP_011514318.1:n.1178-84_1178-75delinsGCC...
XM_011516017.1:c.995-84_995-75delinsGCCCCGTACC XP_011514319.1:n.995-84_995-75delinsGCCCC...
XM_011516018.1:c.968-84_968-75delinsGCCCCGTACC XP_011514320.1:n.968-84_968-75delinsGCCCC...
XM_005250257.2:c.95-84_95-75delinsGCCCCGTACC XP_005250314.1:n.95-84_95-75delinsGCCCCGT...
XM_011516010.2:c.1469-84_1469-75delinsGCCCCGTACC XP_011514312.1:n.1469-84_1469-75delinsGCC...
XM_011516011.2:c.1466-84_1466-75delinsGCCCCGTACC XP_011514313.1:n.1466-84_1466-75delinsGCC...
XM_011516012.2:c.1469-84_1469-75delinsGCCCCGTACC XP_011514314.1:n.1469-84_1469-75delinsGCC...
XM_011516013.2:c.1469-84_1469-75delinsGCCCCGTACC XP_011514315.1:n.1469-84_1469-75delinsGCC...
XM_011516014.2:c.1469-84_1469-75delinsGCCCCGTACC XP_011514316.1:n.1469-84_1469-75delinsGCC...
XM_011516017.2:c.995-84_995-75delinsGCCCCGTACC XP_011514319.1:n.995-84_995-75delinsGCCCC...
XM_011516018.2:c.968-84_968-75delinsGCCCCGTACC XP_011514320.1:n.968-84_968-75delinsGCCCC...
XM_017011951.2:c.1469-84_1469-75delinsGCCCCGTACC XP_016867440.1:n.1469-84_1469-75delinsGCC...
NM_001127231.3:c.1469-84_1469-75delinsGCCCCGTACC NP_001120703.1:n.1469-84_1469-75delinsGCC...
NM_015570.4:c.1469-84_1469-75delinsGCCCCGTACC MANE Select NP_056385.1:n.1469-84_1469-75delinsGCCCCG...