Canonical Allele Identifier: CA77532931

Gene: ROBO2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.77644746C>G , CM000665.2:g.77644746C>G	GRCh38
NC_000003.11:g.77693897C>G , CM000665.1:g.77693897C>G	GRCh37
NC_000003.10:g.77776587C>G	NCBI36
NG_027734.1:g.1743053C>G
NG_027734.2:g.1743053C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332191.13:c.4172C>G	ENSP00000327536.9:p.Pro1391Arg
ENST00000471893.2:c.4163C>G	ENSP00000418190.2:p.Pro1388Arg
ENST00000475334.2:c.4058C>G	ENSP00000418446.2:p.Pro1353Arg
ENST00000490534.2:c.4250C>G	ENSP00000417471.2:p.Pro1417Arg
ENST00000696574.1:c.*920C>G	ENSP00000512729.1:n.*920C>G
ENST00000696593.1:c.4262C>G MANE Select	ENSP00000512738.1:p.Pro1421Arg
ENST00000696629.1:c.4163C>G	ENSP00000512766.1:p.Pro1388Arg
ENST00000696630.1:c.4436C>G	ENSP00000512767.1:p.Pro1479Arg
ENST00000696631.1:c.*2410C>G	ENSP00000512768.1:n.*2410C>G
ENST00000705983.1:c.4103C>G	ENSP00000516193.1:p.Pro1368Arg
ENST00000705984.1:c.518C>G	ENSP00000516194.1:p.Pro173Arg
ENST00000332191.12:c.4160C>G	ENSP00000327536.8:p.Pro1387Arg
ENST00000461745.5:c.3977C>G	ENSP00000417164.1:p.Pro1326Arg
ENST00000470802.1:n.5965C>G
ENST00000473767.5:c.*2421C>G	ENSP00000418117.1:n.*2421C>G
ENST00000475334.1:c.471C>G
ENST00000487694.7:c.4025C>G	ENSP00000417335.2:p.Pro1342Arg
ENST00000490534.1:c.435C>G
ENST00000614793.4:c.3593C>G	ENSP00000480344.1:p.Pro1198Arg
NM_001128929.3:c.4025C>G	NP_001122401.1:p.Pro1342Arg
NM_001290039.1:c.3989C>G	NP_001276968.1:p.Pro1330Arg
NM_001290040.1:c.4172C>G	NP_001276969.1:p.Pro1391Arg
NM_001290065.1:c.2198C>G	NP_001276994.1:p.Pro733Arg
NM_002942.4:c.3977C>G	NP_002933.1:p.Pro1326Arg
XM_011533981.1:c.4640C>G	XP_011532283.1:p.Pro1547Arg
XM_011533982.1:c.4514C>G	XP_011532284.1:p.Pro1505Arg
XM_011533983.1:c.4457C>G	XP_011532285.1:p.Pro1486Arg
XM_011533984.1:c.4184C>G	XP_011532286.1:p.Pro1395Arg
XM_011533985.1:c.4058C>G	XP_011532287.1:p.Pro1353Arg
XM_011533981.2:c.4640C>G	XP_011532283.1:p.Pro1547Arg
XM_017006986.1:c.4571C>G	XP_016862475.1:p.Pro1524Arg
XM_017006987.1:c.4505C>G	XP_016862476.1:p.Pro1502Arg
XM_017006988.1:c.4457C>G	XP_016862477.1:p.Pro1486Arg
XM_017006989.1:c.4445C>G	XP_016862478.1:p.Pro1482Arg
XM_017006990.1:c.4436C>G	XP_016862479.1:p.Pro1479Arg
XM_017006991.1:c.4331C>G	XP_016862480.1:p.Pro1444Arg
XM_017006992.1:c.4310C>G	XP_016862481.1:p.Pro1437Arg
XM_017006993.1:c.4250C>G	XP_016862482.1:p.Pro1417Arg
XM_017006994.1:c.4184C>G	XP_016862483.1:p.Pro1395Arg
XM_017006995.1:c.4175C>G	XP_016862484.1:p.Pro1392Arg
XM_017006996.1:c.4163C>G	XP_016862485.1:p.Pro1388Arg
XM_017006997.1:c.4163C>G	XP_016862486.1:p.Pro1388Arg
XM_017006998.1:c.4115C>G	XP_016862487.1:p.Pro1372Arg
XM_017006999.1:c.4115C>G	XP_016862488.1:p.Pro1372Arg
XM_017007000.1:c.4103C>G	XP_016862489.1:p.Pro1368Arg
XM_017007001.1:c.4058C>G	XP_016862490.1:p.Pro1353Arg
XM_017007002.1:c.4049C>G	XP_016862491.1:p.Pro1350Arg
XM_017007003.1:c.4046C>G	XP_016862492.1:p.Pro1349Arg
XM_017007004.1:c.4037C>G	XP_016862493.1:p.Pro1346Arg
XM_017007005.1:c.4037C>G	XP_016862494.1:p.Pro1346Arg
XM_017007006.1:c.3980C>G	XP_016862495.1:p.Pro1327Arg
NM_001290039.2:c.3989C>G	NP_001276968.1:p.Pro1330Arg
NM_001290040.2:c.4172C>G	NP_001276969.1:p.Pro1391Arg
NM_001290065.2:c.2198C>G	NP_001276994.1:p.Pro733Arg
NM_002942.5:c.3977C>G	NP_002933.1:p.Pro1326Arg
NM_001378190.1:c.4310C>G	NP_001365119.1:p.Pro1437Arg
NM_001378191.1:c.4436C>G	NP_001365120.1:p.Pro1479Arg
NM_001378192.1:c.4331C>G	NP_001365121.1:p.Pro1444Arg
NM_001378193.1:c.4250C>G	NP_001365122.1:p.Pro1417Arg
NM_001378194.1:c.4175C>G	NP_001365123.1:p.Pro1392Arg
NM_001378195.1:c.4163C>G	NP_001365124.1:p.Pro1388Arg
NM_001378196.1:c.4163C>G	NP_001365125.1:p.Pro1388Arg
NM_001378197.1:c.4103C>G	NP_001365126.1:p.Pro1368Arg
NM_001378198.1:c.4058C>G	NP_001365127.1:p.Pro1353Arg
NM_001378199.1:c.4058C>G	NP_001365128.1:p.Pro1353Arg
NM_001378200.1:c.4037C>G	NP_001365129.1:p.Pro1346Arg
NM_001378201.1:c.4037C>G	NP_001365130.1:p.Pro1346Arg
NM_001378202.1:c.3980C>G	NP_001365131.1:p.Pro1327Arg
NM_001378203.1:c.3863C>G	NP_001365132.1:p.Pro1288Arg
NM_001394212.1:c.4445C>G	NP_001381141.1:p.Pro1482Arg
NM_001394213.1:c.4184C>G	NP_001381142.1:p.Pro1395Arg
NM_001394214.1:c.4046C>G	NP_001381143.1:p.Pro1349Arg
NM_001395656.1:c.4262C>G MANE Select	NP_001382585.1:p.Pro1421Arg
NM_001395657.1:c.4172C>G	NP_001382586.1:p.Pro1391Arg