Canonical Allele Identifier: CA1561528379

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87349277_87349278delinsAT , CM000667.2:g.87349277_87349278delinsAT GRCh38
NC_000005.9:g.86645094_86645095delinsAT , CM000667.1:g.86645094_86645095delinsAT GRCh37
NC_000005.8:g.86680850_86680851delinsAT NCBI36
NG_011650.1:g.85944_85945delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.1166_1167delinsAT (RASA1) MANE Select ENSP00000274376.6:p.Tyr389=
ENST00000645953.1:c.*91-30381_*91-30380delinsAT (CCNH) ENSP00000494460.1:n.*91-30381_*91-30380delinsAT
ENST00000274376.10:c.1166_1167delinsAT (RASA1) ENSP00000274376.6:p.Tyr389=
ENST00000456692.6:c.635_636delinsAT (RASA1) ENSP00000411221.2:p.Tyr212=
ENST00000506290.1:c.668_669delinsAT (RASA1) ENSP00000420905.1:p.Tyr223=
ENST00000509953.1:n.269_270delinsAT (RASA1)
ENST00000512763.5:c.665_666delinsAT (RASA1) ENSP00000422008.1:p.Tyr222=
ENST00000515800.6:c.1166_1167delinsAT (RASA1) ENSP00000423395.2:p.Tyr389=
NM_002890.2:c.1166_1167delinsAT (RASA1) NP_002881.1:p.Tyr389=
NM_022650.2:c.635_636delinsAT (RASA1) NP_072179.1:p.Tyr212=
XM_011543525.1:c.1166_1167delinsAT (RASA1) XP_011541827.1:p.Tyr389=
XM_011543526.1:c.1166_1167delinsAT (RASA1) XP_011541828.1:p.Tyr389=
XM_011543527.1:c.1166_1167delinsAT (RASA1) XP_011541829.1:p.Tyr389=
NM_001364075.1:c.934-36483_934-36482delinsAT (CCNH) NP_001351004.1:n.934-36483_934-36482delinsAT
NR_157068.1:n.1448-36483_1448-36482delinsAT (CCNH)
NR_157069.1:n.1041-36483_1041-36482delinsAT (CCNH)
NR_157070.1:n.1205-36483_1205-36482delinsAT (CCNH)
XM_011543525.2:c.1166_1167delinsAT (RASA1) XP_011541827.1:p.Tyr389=
XM_011543527.3:c.1166_1167delinsAT (RASA1) XP_011541829.1:p.Tyr389=
NM_001364075.2:c.934-36483_934-36482delinsAT (CCNH) NP_001351004.1:n.934-36483_934-36482delinsAT
NM_002890.3:c.1166_1167delinsAT (RASA1) MANE Select NP_002881.1:p.Tyr389=
NR_157068.2:n.1448-36483_1448-36482delinsAT (CCNH)
NR_157069.2:n.1041-36483_1041-36482delinsAT (CCNH)
NR_157070.2:n.1205-36483_1205-36482delinsAT (CCNH)
NM_022650.3:c.635_636delinsAT (RASA1) NP_072179.1:p.Tyr212=