Canonical Allele Identifier: CA360380282

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87337974T>G , CM000667.2:g.87337974T>G GRCh38
NC_000005.9:g.86633791T>G , CM000667.1:g.86633791T>G GRCh37
NC_000005.8:g.86669547T>G NCBI36
NG_011650.1:g.74641T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.900T>G (RASA1) MANE Select ENSP00000274376.6:p.Ser300Arg
ENST00000645953.1:c.*91-19077A>C (CCNH) ENSP00000494460.1:n.*91-19077A>C
ENST00000274376.10:c.900T>G (RASA1) ENSP00000274376.6:p.Ser300Arg
ENST00000456692.6:c.369T>G (RASA1) ENSP00000411221.2:p.Ser123Arg
ENST00000506290.1:c.402T>G (RASA1) ENSP00000420905.1:p.Ser134Arg
ENST00000509953.1:n.3T>G (RASA1)
ENST00000512763.5:c.399T>G (RASA1) ENSP00000422008.1:p.Ser133Arg
ENST00000515800.6:c.900T>G (RASA1) ENSP00000423395.2:p.Ser300Arg
NM_002890.2:c.900T>G (RASA1) NP_002881.1:p.Ser300Arg
NM_022650.2:c.369T>G (RASA1) NP_072179.1:p.Ser123Arg
XM_011543525.1:c.900T>G (RASA1) XP_011541827.1:p.Ser300Arg
XM_011543526.1:c.900T>G (RASA1) XP_011541828.1:p.Ser300Arg
XM_011543527.1:c.900T>G (RASA1) XP_011541829.1:p.Ser300Arg
NM_001364075.1:c.934-25179A>C (CCNH) NP_001351004.1:n.934-25179A>C
NR_157068.1:n.1448-25179A>C (CCNH)
NR_157069.1:n.1041-25179A>C (CCNH)
NR_157070.1:n.1205-25179A>C (CCNH)
XM_011543525.2:c.900T>G (RASA1) XP_011541827.1:p.Ser300Arg
XM_011543527.3:c.900T>G (RASA1) XP_011541829.1:p.Ser300Arg
NM_001364075.2:c.934-25179A>C (CCNH) NP_001351004.1:n.934-25179A>C
NM_002890.3:c.900T>G (RASA1) MANE Select NP_002881.1:p.Ser300Arg
NR_157068.2:n.1448-25179A>C (CCNH)
NR_157069.2:n.1041-25179A>C (CCNH)
NR_157070.2:n.1205-25179A>C (CCNH)
NM_022650.3:c.369T>G (RASA1) NP_072179.1:p.Ser123Arg