Canonical Allele Identifier: CA360383696

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87379761T>A , CM000667.2:g.87379761T>A GRCh38
NC_000005.9:g.86675578T>A , CM000667.1:g.86675578T>A GRCh37
NC_000005.8:g.86711334T>A NCBI36
NG_011650.1:g.116428T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.2514T>A (RASA1) MANE Select ENSP00000274376.6:p.Asn838Lys
ENST00000645953.1:c.*90+13009A>T (CCNH) ENSP00000494460.1:n.*90+13009A>T
ENST00000646883.1:c.255-3243A>T (CCNH)
ENST00000274376.10:c.2514T>A (RASA1) ENSP00000274376.6:p.Asn838Lys
ENST00000456692.6:c.1983T>A (RASA1) ENSP00000411221.2:p.Asn661Lys
ENST00000506290.1:c.2016T>A (RASA1) ENSP00000420905.1:p.Asn672Lys
ENST00000512763.5:c.2013T>A (RASA1) ENSP00000422008.1:p.Asn671Lys
ENST00000515800.6:c.*1039T>A (RASA1) ENSP00000423395.2:n.*1039T>A
NM_002890.2:c.2514T>A (RASA1) NP_002881.1:p.Asn838Lys
NM_022650.2:c.1983T>A (RASA1) NP_072179.1:p.Asn661Lys
XM_011543525.1:c.2514T>A (RASA1) XP_011541827.1:p.Asn838Lys
XM_011543526.1:c.2514T>A (RASA1) XP_011541828.1:p.Asn838Lys
NM_001364075.1:c.933+15283A>T (CCNH) NP_001351004.1:n.933+15283A>T
NR_157068.1:n.1447+13009A>T (CCNH)
NR_157069.1:n.1040+13009A>T (CCNH)
NR_157070.1:n.1204+13009A>T (CCNH)
XM_011543525.2:c.2514T>A (RASA1) XP_011541827.1:p.Asn838Lys
NM_001364075.2:c.933+15283A>T (CCNH) NP_001351004.1:n.933+15283A>T
NM_002890.3:c.2514T>A (RASA1) MANE Select NP_002881.1:p.Asn838Lys
NR_157068.2:n.1447+13009A>T (CCNH)
NR_157069.2:n.1040+13009A>T (CCNH)
NR_157070.2:n.1204+13009A>T (CCNH)
NM_022650.3:c.1983T>A (RASA1) NP_072179.1:p.Asn661Lys