Canonical Allele Identifier: CA445200224

Linked Data

gnomAD v4: 5-87379746-A-G
MyVariant Identifiers: chr5:g.86675563A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87379746A>G , CM000667.2:g.87379746A>G GRCh38
NC_000005.9:g.86675563A>G , CM000667.1:g.86675563A>G GRCh37
NC_000005.8:g.86711319A>G NCBI36
NG_011650.1:g.116413A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.2499A>G (RASA1) MANE Select ENSP00000274376.6:p.Ser833=
ENST00000645953.1:c.*90+13024T>C (CCNH) ENSP00000494460.1:n.*90+13024T>C
ENST00000646883.1:c.255-3228T>C (CCNH)
ENST00000274376.10:c.2499A>G (RASA1) ENSP00000274376.6:p.Ser833=
ENST00000456692.6:c.1968A>G (RASA1) ENSP00000411221.2:p.Ser656=
ENST00000506290.1:c.2001A>G (RASA1) ENSP00000420905.1:p.Ser667=
ENST00000512763.5:c.1998A>G (RASA1) ENSP00000422008.1:p.Ser666=
ENST00000515800.6:c.*1024A>G (RASA1) ENSP00000423395.2:n.*1024A>G
NM_002890.2:c.2499A>G (RASA1) NP_002881.1:p.Ser833=
NM_022650.2:c.1968A>G (RASA1) NP_072179.1:p.Ser656=
XM_011543525.1:c.2499A>G (RASA1) XP_011541827.1:p.Ser833=
XM_011543526.1:c.2499A>G (RASA1) XP_011541828.1:p.Ser833=
NM_001364075.1:c.933+15298T>C (CCNH) NP_001351004.1:n.933+15298T>C
NR_157068.1:n.1447+13024T>C (CCNH)
NR_157069.1:n.1040+13024T>C (CCNH)
NR_157070.1:n.1204+13024T>C (CCNH)
XM_011543525.2:c.2499A>G (RASA1) XP_011541827.1:p.Ser833=
NM_001364075.2:c.933+15298T>C (CCNH) NP_001351004.1:n.933+15298T>C
NM_002890.3:c.2499A>G (RASA1) MANE Select NP_002881.1:p.Ser833=
NR_157068.2:n.1447+13024T>C (CCNH)
NR_157069.2:n.1040+13024T>C (CCNH)
NR_157070.2:n.1204+13024T>C (CCNH)
NM_022650.3:c.1968A>G (RASA1) NP_072179.1:p.Ser656=