Canonical Allele Identifier: CA160529084
Gene: AUTS2 HGNC NCBI

Linked Data

dbSNP Id: rs946041123

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69599815C>G , CM000669.2:g.69599815C>G GRCh38
NC_000007.13:g.69064801C>G , CM000669.1:g.69064801C>G GRCh37
NC_000007.12:g.68702737C>G NCBI36
NG_034133.1:g.5897C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342771.10:c.162C>G MANE Select ENSP00000344087.4:p.Ser54=
ENST00000403018.3:c.162C>G ENSP00000385572.2:p.Ser54=
ENST00000644939.1:c.162C>G ENSP00000496726.1:p.Ser54=
ENST00000342771.8:c.162C>G ENSP00000344087.4:p.Ser54=
ENST00000403018.2:c.162C>G ENSP00000385572.2:p.Ser54=
ENST00000406775.6:c.162C>G ENSP00000385263.2:p.Ser54=
NM_001127231.2:c.162C>G NP_001120703.1:p.Ser54=
NM_001127232.2:c.162C>G NP_001120704.1:p.Ser54=
NM_015570.3:c.162C>G NP_056385.1:p.Ser54=
XM_011516010.1:c.162C>G XP_011514312.1:p.Ser54=
XM_011516011.1:c.162C>G XP_011514313.1:p.Ser54=
XM_011516012.1:c.162C>G XP_011514314.1:p.Ser54=
XM_011516013.1:c.162C>G XP_011514315.1:p.Ser54=
XM_011516014.1:c.162C>G XP_011514316.1:p.Ser54=
XM_011516015.1:c.162C>G XP_011514317.1:p.Ser54=
XM_011516010.2:c.162C>G XP_011514312.1:p.Ser54=
XM_011516011.2:c.162C>G XP_011514313.1:p.Ser54=
XM_011516012.2:c.162C>G XP_011514314.1:p.Ser54=
XM_011516013.2:c.162C>G XP_011514315.1:p.Ser54=
XM_011516014.2:c.162C>G XP_011514316.1:p.Ser54=
XM_017011951.2:c.162C>G XP_016867440.1:p.Ser54=
NM_001127231.3:c.162C>G NP_001120703.1:p.Ser54=
NM_001127232.3:c.162C>G NP_001120704.1:p.Ser54=
NM_015570.4:c.162C>G MANE Select NP_056385.1:p.Ser54=