Canonical Allele Identifier: CA160034414

Gene: AUTS2

Linked Data

• dbSNP Id: rs141563472
• gnomAD v3: 7-70777269-C-A
• gnomAD v4: 7-70777269-C-A
• MyVariant Identifiers: chr7:g.70242255C>A (hg19) ; chr7:g.70777269C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.70777269C>A , CM000669.2:g.70777269C>A	GRCh38
NC_000007.13:g.70242255C>A , CM000669.1:g.70242255C>A	GRCh37
NC_000007.12:g.69880191C>A	NCBI36
NG_034133.1:g.1183351C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700075.1:c.72+95C>A	ENSP00000514784.1:n.72+95C>A
ENST00000342771.10:c.2004+95C>A MANE Select	ENSP00000344087.4:n.2004+95C>A
ENST00000439256.2:c.145+52C>A	ENSP00000407058.2:n.145+52C>A
ENST00000443672.2:c.339+95C>A	ENSP00000393548.2:n.339+95C>A
ENST00000449547.6:c.97+95C>A
ENST00000464768.2:n.672+95C>A
ENST00000644359.1:c.585+95C>A	ENSP00000494561.1:n.585+95C>A
ENST00000644506.1:c.630+95C>A	ENSP00000496672.1:n.630+95C>A
ENST00000644939.1:c.2001+95C>A	ENSP00000496726.1:n.2001+95C>A
ENST00000646136.1:n.315+95C>A
ENST00000647140.1:c.869+95C>A
ENST00000342771.8:c.2004+95C>A	ENSP00000344087.4:n.2004+95C>A
ENST00000406775.6:c.1932+95C>A	ENSP00000385263.2:n.1932+95C>A
ENST00000439256.1:c.145+52C>A
ENST00000464768.1:n.670+95C>A
ENST00000465899.1:n.501+95C>A
ENST00000498384.5:n.372+95C>A
ENST00000611706.4:c.1260+95C>A	ENSP00000478134.1:n.1260+95C>A
ENST00000615871.4:c.1188+95C>A	ENSP00000479325.1:n.1188+95C>A
NM_001127231.2:c.1932+95C>A	NP_001120703.1:n.1932+95C>A
NM_015570.3:c.2004+95C>A	NP_056385.1:n.2004+95C>A
XM_005250257.1:c.651+95C>A	XP_005250314.1:n.651+95C>A
XM_011516010.1:c.2025+95C>A	XP_011514312.1:n.2025+95C>A
XM_011516011.1:c.2022+95C>A	XP_011514313.1:n.2022+95C>A
XM_011516012.1:c.1959+95C>A	XP_011514314.1:n.1959+95C>A
XM_011516013.1:c.1953+95C>A	XP_011514315.1:n.1953+95C>A
XM_011516014.1:c.1923+95C>A	XP_011514316.1:n.1923+95C>A
XM_011516015.1:c.1761+95C>A	XP_011514317.1:n.1761+95C>A
XM_011516016.1:c.1734+95C>A	XP_011514318.1:n.1734+95C>A
XM_011516017.1:c.1551+95C>A	XP_011514319.1:n.1551+95C>A
XM_011516018.1:c.1524+95C>A	XP_011514320.1:n.1524+95C>A
XM_005250257.2:c.651+95C>A	XP_005250314.1:n.651+95C>A
XM_011516010.2:c.2025+95C>A	XP_011514312.1:n.2025+95C>A
XM_011516011.2:c.2022+95C>A	XP_011514313.1:n.2022+95C>A
XM_011516012.2:c.1959+95C>A	XP_011514314.1:n.1959+95C>A
XM_011516013.2:c.1953+95C>A	XP_011514315.1:n.1953+95C>A
XM_011516014.2:c.1923+95C>A	XP_011514316.1:n.1923+95C>A
XM_011516017.2:c.1551+95C>A	XP_011514319.1:n.1551+95C>A
XM_011516018.2:c.1524+95C>A	XP_011514320.1:n.1524+95C>A
XM_017011951.2:c.2025+95C>A	XP_016867440.1:n.2025+95C>A
NM_001127231.3:c.1932+95C>A	NP_001120703.1:n.1932+95C>A
NM_015570.4:c.2004+95C>A MANE Select	NP_056385.1:n.2004+95C>A