Canonical Allele Identifier: CA367668828
Community Standard Title: NM_015570.4(AUTS2):c.1557C>G (p.Tyr519Ter)
Gene: AUTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70766202C>G , CM000669.2:g.70766202C>G GRCh38
NC_000007.13:g.70231188C>G , CM000669.1:g.70231188C>G GRCh37
NC_000007.12:g.69869124C>G NCBI36
NG_034133.1:g.1172284C>G

Transcript Alleles

HGVS Amino-acid Change
NM_015570.4:c.1557C>G MANE Select NP_056385.1:p.Tyr519Ter
ENST00000342771.10:c.1557C>G MANE Select ENSP00000344087.4:p.Tyr519Ter
NM_001127231.2:c.1557C>G NP_001120703.1:p.Tyr519Ter
NM_001127231.3:c.1557C>G NP_001120703.1:p.Tyr519Ter
NM_015570.3:c.1557C>G NP_056385.1:p.Tyr519Ter
ENST00000342771.8:c.1557C>G ENSP00000344087.4:p.Tyr519Ter
ENST00000406775.6:c.1557C>G ENSP00000385263.2:p.Tyr519Ter
ENST00000443672.1:c.182C>G
ENST00000443672.2:c.-109C>G ENSP00000393548.2:n.-109C>G
ENST00000481994.1:n.164C>G
ENST00000611706.4:c.813C>G ENSP00000478134.1:p.Tyr271Ter
ENST00000615871.4:c.813C>G ENSP00000479325.1:p.Tyr271Ter
ENST00000644359.1:c.183C>G ENSP00000494561.1:p.Tyr61Ter
ENST00000644506.1:c.183C>G ENSP00000496672.1:p.Tyr61Ter
ENST00000644939.1:c.1554C>G ENSP00000496726.1:p.Tyr518Ter
ENST00000647140.1:c.401C>G
ENST00000656200.1:c.183C>G ENSP00000499508.1:p.Tyr61Ter
XM_005250257.1:c.183C>G XP_005250314.1:p.Tyr61Ter
XM_005250257.2:c.183C>G XP_005250314.1:p.Tyr61Ter
XM_011516010.1:c.1557C>G XP_011514312.1:p.Tyr519Ter
XM_011516010.2:c.1557C>G XP_011514312.1:p.Tyr519Ter
XM_011516011.1:c.1554C>G XP_011514313.1:p.Tyr518Ter
XM_011516011.2:c.1554C>G XP_011514313.1:p.Tyr518Ter
XM_011516012.1:c.1557C>G XP_011514314.1:p.Tyr519Ter
XM_011516012.2:c.1557C>G XP_011514314.1:p.Tyr519Ter
XM_011516013.1:c.1557C>G XP_011514315.1:p.Tyr519Ter
XM_011516013.2:c.1557C>G XP_011514315.1:p.Tyr519Ter
XM_011516014.1:c.1557C>G XP_011514316.1:p.Tyr519Ter
XM_011516014.2:c.1557C>G XP_011514316.1:p.Tyr519Ter
XM_011516015.1:c.1557C>G XP_011514317.1:p.Tyr519Ter
XM_011516016.1:c.1266C>G XP_011514318.1:p.Tyr422Ter
XM_011516017.1:c.1083C>G XP_011514319.1:p.Tyr361Ter
XM_011516017.2:c.1083C>G XP_011514319.1:p.Tyr361Ter
XM_011516018.1:c.1056C>G XP_011514320.1:p.Tyr352Ter
XM_011516018.2:c.1056C>G XP_011514320.1:p.Tyr352Ter
XM_017011951.2:c.1557C>G XP_016867440.1:p.Tyr519Ter