Canonical Allele Identifier: CA360383636

Linked Data

gnomAD v3: 5-87379751-T-A
gnomAD v4: 5-87379751-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87379751T>A , CM000667.2:g.87379751T>A GRCh38
NC_000005.9:g.86675568T>A , CM000667.1:g.86675568T>A GRCh37
NC_000005.8:g.86711324T>A NCBI36
NG_011650.1:g.116418T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.2504T>A (RASA1) MANE Select ENSP00000274376.6:p.Leu835Ter
ENST00000645953.1:c.*90+13019A>T (CCNH) ENSP00000494460.1:n.*90+13019A>T
ENST00000646883.1:c.255-3233A>T (CCNH)
ENST00000274376.10:c.2504T>A (RASA1) ENSP00000274376.6:p.Leu835Ter
ENST00000456692.6:c.1973T>A (RASA1) ENSP00000411221.2:p.Leu658Ter
ENST00000506290.1:c.2006T>A (RASA1) ENSP00000420905.1:p.Leu669Ter
ENST00000512763.5:c.2003T>A (RASA1) ENSP00000422008.1:p.Leu668Ter
ENST00000515800.6:c.*1029T>A (RASA1) ENSP00000423395.2:n.*1029T>A
NM_002890.2:c.2504T>A (RASA1) NP_002881.1:p.Leu835Ter
NM_022650.2:c.1973T>A (RASA1) NP_072179.1:p.Leu658Ter
XM_011543525.1:c.2504T>A (RASA1) XP_011541827.1:p.Leu835Ter
XM_011543526.1:c.2504T>A (RASA1) XP_011541828.1:p.Leu835Ter
NM_001364075.1:c.933+15293A>T (CCNH) NP_001351004.1:n.933+15293A>T
NR_157068.1:n.1447+13019A>T (CCNH)
NR_157069.1:n.1040+13019A>T (CCNH)
NR_157070.1:n.1204+13019A>T (CCNH)
XM_011543525.2:c.2504T>A (RASA1) XP_011541827.1:p.Leu835Ter
NM_001364075.2:c.933+15293A>T (CCNH) NP_001351004.1:n.933+15293A>T
NM_002890.3:c.2504T>A (RASA1) MANE Select NP_002881.1:p.Leu835Ter
NR_157068.2:n.1447+13019A>T (CCNH)
NR_157069.2:n.1040+13019A>T (CCNH)
NR_157070.2:n.1204+13019A>T (CCNH)
NM_022650.3:c.1973T>A (RASA1) NP_072179.1:p.Leu658Ter