Canonical Allele Identifier: CA1716145263
Gene: AUTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70777035_70777036delinsTG , CM000669.2:g.70777035_70777036delinsTG GRCh38
NC_000007.13:g.70242021_70242022delinsTG , CM000669.1:g.70242021_70242022delinsTG GRCh37
NC_000007.12:g.69879957_69879958delinsTG NCBI36
NG_034133.1:g.1183117_1183118delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000342771.10:c.1933-68_1933-67delinsTG MANE Select ENSP00000344087.4:n.1933-68_1933-67delinsTG
ENST00000439256.2:c.31-68_31-67delinsTG ENSP00000407058.2:n.31-68_31-67delinsTG
ENST00000443672.2:c.268-68_268-67delinsTG ENSP00000393548.2:n.268-68_268-67delinsTG
ENST00000449547.6:c.26-68_26-67delinsTG
ENST00000464768.2:n.601-68_601-67delinsTG
ENST00000644359.1:c.514-68_514-67delinsTG ENSP00000494561.1:n.514-68_514-67delinsTG
ENST00000644506.1:c.559-68_559-67delinsTG ENSP00000496672.1:n.559-68_559-67delinsTG
ENST00000644939.1:c.1930-68_1930-67delinsTG ENSP00000496726.1:n.1930-68_1930-67delinsTG
ENST00000644949.1:c.264-68_264-67delinsTG
ENST00000646136.1:n.244-68_244-67delinsTG
ENST00000647140.1:c.798-68_798-67delinsTG
ENST00000342771.8:c.1933-68_1933-67delinsTG ENSP00000344087.4:n.1933-68_1933-67delinsTG
ENST00000406775.6:c.1861-68_1861-67delinsTG ENSP00000385263.2:n.1861-68_1861-67delinsTG
ENST00000439256.1:c.31-68_31-67delinsTG
ENST00000443672.1:c.513-68_513-67delinsTG
ENST00000464768.1:n.599-68_599-67delinsTG
ENST00000465899.1:n.362_363delinsTG
ENST00000498384.5:n.301-68_301-67delinsTG
ENST00000611706.4:c.1189-68_1189-67delinsTG ENSP00000478134.1:n.1189-68_1189-67delinsTG
ENST00000615871.4:c.1117-68_1117-67delinsTG ENSP00000479325.1:n.1117-68_1117-67delinsTG
NM_001127231.2:c.1861-68_1861-67delinsTG NP_001120703.1:n.1861-68_1861-67delinsTG
NM_015570.3:c.1933-68_1933-67delinsTG NP_056385.1:n.1933-68_1933-67delinsTG
XM_005250257.1:c.580-68_580-67delinsTG XP_005250314.1:n.580-68_580-67delinsTG
XM_011516010.1:c.1954-68_1954-67delinsTG XP_011514312.1:n.1954-68_1954-67delinsTG
XM_011516011.1:c.1951-68_1951-67delinsTG XP_011514313.1:n.1951-68_1951-67delinsTG
XM_011516012.1:c.1888-68_1888-67delinsTG XP_011514314.1:n.1888-68_1888-67delinsTG
XM_011516013.1:c.1882-68_1882-67delinsTG XP_011514315.1:n.1882-68_1882-67delinsTG
XM_011516014.1:c.1852-68_1852-67delinsTG XP_011514316.1:n.1852-68_1852-67delinsTG
XM_011516015.1:c.1690-68_1690-67delinsTG XP_011514317.1:n.1690-68_1690-67delinsTG
XM_011516016.1:c.1663-68_1663-67delinsTG XP_011514318.1:n.1663-68_1663-67delinsTG
XM_011516017.1:c.1480-68_1480-67delinsTG XP_011514319.1:n.1480-68_1480-67delinsTG
XM_011516018.1:c.1453-68_1453-67delinsTG XP_011514320.1:n.1453-68_1453-67delinsTG
XM_005250257.2:c.580-68_580-67delinsTG XP_005250314.1:n.580-68_580-67delinsTG
XM_011516010.2:c.1954-68_1954-67delinsTG XP_011514312.1:n.1954-68_1954-67delinsTG
XM_011516011.2:c.1951-68_1951-67delinsTG XP_011514313.1:n.1951-68_1951-67delinsTG
XM_011516012.2:c.1888-68_1888-67delinsTG XP_011514314.1:n.1888-68_1888-67delinsTG
XM_011516013.2:c.1882-68_1882-67delinsTG XP_011514315.1:n.1882-68_1882-67delinsTG
XM_011516014.2:c.1852-68_1852-67delinsTG XP_011514316.1:n.1852-68_1852-67delinsTG
XM_011516017.2:c.1480-68_1480-67delinsTG XP_011514319.1:n.1480-68_1480-67delinsTG
XM_011516018.2:c.1453-68_1453-67delinsTG XP_011514320.1:n.1453-68_1453-67delinsTG
XM_017011951.2:c.1954-68_1954-67delinsTG XP_016867440.1:n.1954-68_1954-67delinsTG
NM_001127231.3:c.1861-68_1861-67delinsTG NP_001120703.1:n.1861-68_1861-67delinsTG
NM_015570.4:c.1933-68_1933-67delinsTG MANE Select NP_056385.1:n.1933-68_1933-67delinsTG