Canonical Allele Identifier: CA1561579205

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331437_87331450delinsATCGGAGGCCAGGG , CM000667.2:g.87331437_87331450delinsATCGGAGGCCAGGG GRCh38
NC_000005.9:g.86627254_86627267delinsATCGGAGGCCAGGG , CM000667.1:g.86627254_86627267delinsATCGGAGGCCAGGG GRCh37
NC_000005.8:g.86663010_86663023delinsATCGGAGGCCAGGG NCBI36
NG_011650.1:g.68104_68117delinsATCGGAGGCCAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.629_642delinsATCGGAGGCCAGGG (RASA1) MANE Select ENSP00000274376.6:p.Asp210=
ENST00000645953.1:c.*91-12553_*91-12540delinsCCCTGGCCTCCGAT (CCNH) ENSP00000494460.1:n.*91-12553_*91-12540delinsCCCTGGCCTCCGAT
ENST00000274376.10:c.629_642delinsATCGGAGGCCAGGG (RASA1) ENSP00000274376.6:p.Asp210=
ENST00000456692.6:c.98_111delinsATCGGAGGCCAGGG (RASA1) ENSP00000411221.2:p.Asp33=
ENST00000506290.1:c.131_144delinsATCGGAGGCCAGGG (RASA1) ENSP00000420905.1:p.Asp44=
ENST00000512763.5:c.128_141delinsATCGGAGGCCAGGG (RASA1) ENSP00000422008.1:p.Asp43=
ENST00000515800.6:c.629_642delinsATCGGAGGCCAGGG (RASA1) ENSP00000423395.2:p.Asp210=
NM_002890.2:c.629_642delinsATCGGAGGCCAGGG (RASA1) NP_002881.1:p.Asp210=
NM_022650.2:c.98_111delinsATCGGAGGCCAGGG (RASA1) NP_072179.1:p.Asp33=
XM_011543525.1:c.629_642delinsATCGGAGGCCAGGG (RASA1) XP_011541827.1:p.Asp210=
XM_011543526.1:c.629_642delinsATCGGAGGCCAGGG (RASA1) XP_011541828.1:p.Asp210=
XM_011543527.1:c.629_642delinsATCGGAGGCCAGGG (RASA1) XP_011541829.1:p.Asp210=
NM_001364075.1:c.934-18655_934-18642delinsCCCTGGCCTCCGAT (CCNH) NP_001351004.1:n.934-18655_934-18642delinsCCCTGGCCTCCGAT
NR_157068.1:n.1448-18655_1448-18642delinsCCCTGGCCTCCGAT (CCNH)
NR_157069.1:n.1041-18655_1041-18642delinsCCCTGGCCTCCGAT (CCNH)
NR_157070.1:n.1205-18655_1205-18642delinsCCCTGGCCTCCGAT (CCNH)
XM_011543525.2:c.629_642delinsATCGGAGGCCAGGG (RASA1) XP_011541827.1:p.Asp210=
XM_011543527.3:c.629_642delinsATCGGAGGCCAGGG (RASA1) XP_011541829.1:p.Asp210=
NM_001364075.2:c.934-18655_934-18642delinsCCCTGGCCTCCGAT (CCNH) NP_001351004.1:n.934-18655_934-18642delinsCCCTGGCCTCCGAT
NM_002890.3:c.629_642delinsATCGGAGGCCAGGG (RASA1) MANE Select NP_002881.1:p.Asp210=
NR_157068.2:n.1448-18655_1448-18642delinsCCCTGGCCTCCGAT (CCNH)
NR_157069.2:n.1041-18655_1041-18642delinsCCCTGGCCTCCGAT (CCNH)
NR_157070.2:n.1205-18655_1205-18642delinsCCCTGGCCTCCGAT (CCNH)
NM_022650.3:c.98_111delinsATCGGAGGCCAGGG (RASA1) NP_072179.1:p.Asp33=