Canonical Allele Identifier: CA367667449
Gene: AUTS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70763034G>C , CM000669.2:g.70763034G>C GRCh38
NC_000007.13:g.70228020G>C , CM000669.1:g.70228020G>C GRCh37
NC_000007.12:g.69865956G>C NCBI36
NG_034133.1:g.1169116G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000342771.10:c.907G>C MANE Select ENSP00000344087.4:p.Ala303Pro
ENST00000443672.2:c.-197-3080G>C ENSP00000393548.2:n.-197-3080G>C
ENST00000644359.1:c.-465G>C ENSP00000494561.1:n.-465G>C
ENST00000644506.1:c.-465G>C ENSP00000496672.1:n.-465G>C
ENST00000644939.1:c.907G>C ENSP00000496726.1:p.Ala303Pro
ENST00000656200.1:c.-468G>C ENSP00000499508.1:n.-468G>C
ENST00000342771.8:c.907G>C ENSP00000344087.4:p.Ala303Pro
ENST00000406775.6:c.907G>C ENSP00000385263.2:p.Ala303Pro
ENST00000416482.1:c.248G>C
ENST00000611706.4:c.163G>C ENSP00000478134.1:p.Ala55Pro
ENST00000615871.4:c.163G>C ENSP00000479325.1:p.Ala55Pro
NM_001127231.2:c.907G>C NP_001120703.1:p.Ala303Pro
NM_015570.3:c.907G>C NP_056385.1:p.Ala303Pro
XM_011516010.1:c.907G>C XP_011514312.1:p.Ala303Pro
XM_011516011.1:c.907G>C XP_011514313.1:p.Ala303Pro
XM_011516012.1:c.907G>C XP_011514314.1:p.Ala303Pro
XM_011516013.1:c.907G>C XP_011514315.1:p.Ala303Pro
XM_011516014.1:c.907G>C XP_011514316.1:p.Ala303Pro
XM_011516015.1:c.907G>C XP_011514317.1:p.Ala303Pro
XM_011516016.1:c.616G>C XP_011514318.1:p.Ala206Pro
XM_011516017.1:c.433G>C XP_011514319.1:p.Ala145Pro
XM_011516018.1:c.406G>C XP_011514320.1:p.Ala136Pro
XM_011516010.2:c.907G>C XP_011514312.1:p.Ala303Pro
XM_011516011.2:c.907G>C XP_011514313.1:p.Ala303Pro
XM_011516012.2:c.907G>C XP_011514314.1:p.Ala303Pro
XM_011516013.2:c.907G>C XP_011514315.1:p.Ala303Pro
XM_011516014.2:c.907G>C XP_011514316.1:p.Ala303Pro
XM_011516017.2:c.433G>C XP_011514319.1:p.Ala145Pro
XM_011516018.2:c.406G>C XP_011514320.1:p.Ala136Pro
XM_017011951.2:c.907G>C XP_016867440.1:p.Ala303Pro
NM_001127231.3:c.907G>C NP_001120703.1:p.Ala303Pro
NM_015570.4:c.907G>C MANE Select NP_056385.1:p.Ala303Pro