Canonical Allele Identifier: CA367669716

Gene: AUTS2

Linked Data

• MyVariant Identifiers: chr7:g.70242092C>G (hg19) ; chr7:g.70777106C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70777106C>G , CM000669.2:g.70777106C>G	GRCh38
NC_000007.13:g.70242092C>G , CM000669.1:g.70242092C>G	GRCh37
NC_000007.12:g.69880028C>G	NCBI36
NG_034133.1:g.1183188C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700075.1:c.4C>G	ENSP00000514784.1:p.Pro2Ala
ENST00000342771.10:c.1936C>G MANE Select	ENSP00000344087.4:p.Pro646Ala
ENST00000439256.2:c.34C>G	ENSP00000407058.2:p.Pro12Ala
ENST00000443672.2:c.271C>G	ENSP00000393548.2:p.Pro91Ala
ENST00000449547.6:c.29C>G
ENST00000464768.2:n.604C>G
ENST00000644359.1:c.517C>G	ENSP00000494561.1:p.Pro173Ala
ENST00000644506.1:c.562C>G	ENSP00000496672.1:p.Pro188Ala
ENST00000644939.1:c.1933C>G	ENSP00000496726.1:p.Pro645Ala
ENST00000644949.1:c.267C>G
ENST00000646136.1:n.247C>G
ENST00000647140.1:c.801C>G
ENST00000342771.8:c.1936C>G	ENSP00000344087.4:p.Pro646Ala
ENST00000406775.6:c.1864C>G	ENSP00000385263.2:p.Pro622Ala
ENST00000439256.1:c.34C>G
ENST00000443672.1:c.516C>G
ENST00000464768.1:n.602C>G
ENST00000465899.1:n.433C>G
ENST00000498384.5:n.304C>G
ENST00000611706.4:c.1192C>G	ENSP00000478134.1:p.Pro398Ala
ENST00000615871.4:c.1120C>G	ENSP00000479325.1:p.Pro374Ala
NM_001127231.2:c.1864C>G	NP_001120703.1:p.Pro622Ala
NM_015570.3:c.1936C>G	NP_056385.1:p.Pro646Ala
XM_005250257.1:c.583C>G	XP_005250314.1:p.Pro195Ala
XM_011516010.1:c.1957C>G	XP_011514312.1:p.Pro653Ala
XM_011516011.1:c.1954C>G	XP_011514313.1:p.Pro652Ala
XM_011516012.1:c.1891C>G	XP_011514314.1:p.Pro631Ala
XM_011516013.1:c.1885C>G	XP_011514315.1:p.Pro629Ala
XM_011516014.1:c.1855C>G	XP_011514316.1:p.Pro619Ala
XM_011516015.1:c.1693C>G	XP_011514317.1:p.Pro565Ala
XM_011516016.1:c.1666C>G	XP_011514318.1:p.Pro556Ala
XM_011516017.1:c.1483C>G	XP_011514319.1:p.Pro495Ala
XM_011516018.1:c.1456C>G	XP_011514320.1:p.Pro486Ala
XM_005250257.2:c.583C>G	XP_005250314.1:p.Pro195Ala
XM_011516010.2:c.1957C>G	XP_011514312.1:p.Pro653Ala
XM_011516011.2:c.1954C>G	XP_011514313.1:p.Pro652Ala
XM_011516012.2:c.1891C>G	XP_011514314.1:p.Pro631Ala
XM_011516013.2:c.1885C>G	XP_011514315.1:p.Pro629Ala
XM_011516014.2:c.1855C>G	XP_011514316.1:p.Pro619Ala
XM_011516017.2:c.1483C>G	XP_011514319.1:p.Pro495Ala
XM_011516018.2:c.1456C>G	XP_011514320.1:p.Pro486Ala
XM_017011951.2:c.1957C>G	XP_016867440.1:p.Pro653Ala
NM_001127231.3:c.1864C>G	NP_001120703.1:p.Pro622Ala
NM_015570.4:c.1936C>G MANE Select	NP_056385.1:p.Pro646Ala