Canonical Allele Identifier: CA918035678

Gene: AUTS2

Linked Data

• ClinVar Variation Id: 3132361
• ClinVar RCV Id: RCV004421289
• dbSNP Id: rs1562747728

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69599871del , CM000669.2:g.69599871del	GRCh38
NC_000007.13:g.69064857del , CM000669.1:g.69064857del	GRCh37
NC_000007.12:g.68702793del	NCBI36
NG_034133.1:g.5953del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342771.10:c.218del MANE Select	ENSP00000344087.4:p.Pro73ArgfsTer21
ENST00000403018.3:c.218del	ENSP00000385572.2:p.Pro73ArgfsTer21
ENST00000644939.1:c.218del	ENSP00000496726.1:p.Pro73ArgfsTer21
ENST00000342771.8:c.218del	ENSP00000344087.4:p.Pro73ArgfsTer21
ENST00000403018.2:c.218del	ENSP00000385572.2:p.Pro73ArgfsTer21
ENST00000406775.6:c.218del	ENSP00000385263.2:p.Pro73ArgfsTer21
NM_001127231.2:c.218del	NP_001120703.1:p.Pro73ArgfsTer21
NM_001127232.2:c.218del	NP_001120704.1:p.Pro73ArgfsTer21
NM_015570.3:c.218del	NP_056385.1:p.Pro73ArgfsTer21
XM_011516010.1:c.218del	XP_011514312.1:p.Pro73ArgfsTer21
XM_011516011.1:c.218del	XP_011514313.1:p.Pro73ArgfsTer21
XM_011516012.1:c.218del	XP_011514314.1:p.Pro73ArgfsTer21
XM_011516013.1:c.218del	XP_011514315.1:p.Pro73ArgfsTer21
XM_011516014.1:c.218del	XP_011514316.1:p.Pro73ArgfsTer21
XM_011516015.1:c.218del	XP_011514317.1:p.Pro73ArgfsTer21
XM_011516010.2:c.218del	XP_011514312.1:p.Pro73ArgfsTer21
XM_011516011.2:c.218del	XP_011514313.1:p.Pro73ArgfsTer21
XM_011516012.2:c.218del	XP_011514314.1:p.Pro73ArgfsTer21
XM_011516013.2:c.218del	XP_011514315.1:p.Pro73ArgfsTer21
XM_011516014.2:c.218del	XP_011514316.1:p.Pro73ArgfsTer21
XM_017011951.2:c.218del	XP_016867440.1:p.Pro73ArgfsTer21
NM_001127231.3:c.218del	NP_001120703.1:p.Pro73ArgfsTer21
NM_001127232.3:c.218del	NP_001120704.1:p.Pro73ArgfsTer21
NM_015570.4:c.218del MANE Select	NP_056385.1:p.Pro73ArgfsTer21