Canonical Allele Identifier: CA367668695
Gene: AUTS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70766138T>C , CM000669.2:g.70766138T>C GRCh38
NC_000007.13:g.70231124T>C , CM000669.1:g.70231124T>C GRCh37
NC_000007.12:g.69869060T>C NCBI36
NG_034133.1:g.1172220T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342771.10:c.1493T>C MANE Select ENSP00000344087.4:p.Leu498Pro
ENST00000443672.2:c.-173T>C ENSP00000393548.2:n.-173T>C
ENST00000644359.1:c.119T>C ENSP00000494561.1:p.Leu40Pro
ENST00000644506.1:c.119T>C ENSP00000496672.1:p.Leu40Pro
ENST00000644939.1:c.1490T>C ENSP00000496726.1:p.Leu497Pro
ENST00000647140.1:c.337T>C
ENST00000656200.1:c.119T>C ENSP00000499508.1:p.Leu40Pro
ENST00000342771.8:c.1493T>C ENSP00000344087.4:p.Leu498Pro
ENST00000406775.6:c.1493T>C ENSP00000385263.2:p.Leu498Pro
ENST00000443672.1:c.118T>C
ENST00000481994.1:n.100T>C
ENST00000611706.4:c.749T>C ENSP00000478134.1:p.Leu250Pro
ENST00000615871.4:c.749T>C ENSP00000479325.1:p.Leu250Pro
NM_001127231.2:c.1493T>C NP_001120703.1:p.Leu498Pro
NM_015570.3:c.1493T>C NP_056385.1:p.Leu498Pro
XM_005250257.1:c.119T>C XP_005250314.1:p.Leu40Pro
XM_011516010.1:c.1493T>C XP_011514312.1:p.Leu498Pro
XM_011516011.1:c.1490T>C XP_011514313.1:p.Leu497Pro
XM_011516012.1:c.1493T>C XP_011514314.1:p.Leu498Pro
XM_011516013.1:c.1493T>C XP_011514315.1:p.Leu498Pro
XM_011516014.1:c.1493T>C XP_011514316.1:p.Leu498Pro
XM_011516015.1:c.1493T>C XP_011514317.1:p.Leu498Pro
XM_011516016.1:c.1202T>C XP_011514318.1:p.Leu401Pro
XM_011516017.1:c.1019T>C XP_011514319.1:p.Leu340Pro
XM_011516018.1:c.992T>C XP_011514320.1:p.Leu331Pro
XM_005250257.2:c.119T>C XP_005250314.1:p.Leu40Pro
XM_011516010.2:c.1493T>C XP_011514312.1:p.Leu498Pro
XM_011516011.2:c.1490T>C XP_011514313.1:p.Leu497Pro
XM_011516012.2:c.1493T>C XP_011514314.1:p.Leu498Pro
XM_011516013.2:c.1493T>C XP_011514315.1:p.Leu498Pro
XM_011516014.2:c.1493T>C XP_011514316.1:p.Leu498Pro
XM_011516017.2:c.1019T>C XP_011514319.1:p.Leu340Pro
XM_011516018.2:c.992T>C XP_011514320.1:p.Leu331Pro
XM_017011951.2:c.1493T>C XP_016867440.1:p.Leu498Pro
NM_001127231.3:c.1493T>C NP_001120703.1:p.Leu498Pro
NM_015570.4:c.1493T>C MANE Select NP_056385.1:p.Leu498Pro