Canonical Allele Identifier: CA360383574

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87379739G>A , CM000667.2:g.87379739G>A GRCh38
NC_000005.9:g.86675556G>A , CM000667.1:g.86675556G>A GRCh37
NC_000005.8:g.86711312G>A NCBI36
NG_011650.1:g.116406G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.2492G>A (RASA1) MANE Select ENSP00000274376.6:p.Ser831Asn
ENST00000645953.1:c.*90+13031C>T (CCNH) ENSP00000494460.1:n.*90+13031C>T
ENST00000646883.1:c.255-3221C>T (CCNH)
ENST00000274376.10:c.2492G>A (RASA1) ENSP00000274376.6:p.Ser831Asn
ENST00000456692.6:c.1961G>A (RASA1) ENSP00000411221.2:p.Ser654Asn
ENST00000506290.1:c.1994G>A (RASA1) ENSP00000420905.1:p.Ser665Asn
ENST00000512763.5:c.1991G>A (RASA1) ENSP00000422008.1:p.Ser664Asn
ENST00000515800.6:c.*1017G>A (RASA1) ENSP00000423395.2:n.*1017G>A
NM_002890.2:c.2492G>A (RASA1) NP_002881.1:p.Ser831Asn
NM_022650.2:c.1961G>A (RASA1) NP_072179.1:p.Ser654Asn
XM_011543525.1:c.2492G>A (RASA1) XP_011541827.1:p.Ser831Asn
XM_011543526.1:c.2492G>A (RASA1) XP_011541828.1:p.Ser831Asn
NM_001364075.1:c.933+15305C>T (CCNH) NP_001351004.1:n.933+15305C>T
NR_157068.1:n.1447+13031C>T (CCNH)
NR_157069.1:n.1040+13031C>T (CCNH)
NR_157070.1:n.1204+13031C>T (CCNH)
XM_011543525.2:c.2492G>A (RASA1) XP_011541827.1:p.Ser831Asn
NM_001364075.2:c.933+15305C>T (CCNH) NP_001351004.1:n.933+15305C>T
NM_002890.3:c.2492G>A (RASA1) MANE Select NP_002881.1:p.Ser831Asn
NR_157068.2:n.1447+13031C>T (CCNH)
NR_157069.2:n.1040+13031C>T (CCNH)
NR_157070.2:n.1204+13031C>T (CCNH)
NM_022650.3:c.1961G>A (RASA1) NP_072179.1:p.Ser654Asn