Canonical Allele Identifier: CA1561615990

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87389551A= , CM000667.2:g.87389551A= GRCh38
NC_000005.9:g.86685368A= , CM000667.1:g.86685368A= GRCh37
NC_000005.8:g.86721124A= NCBI36
NG_011650.1:g.126218A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.3060+24A= (RASA1) MANE Select ENSP00000274376.6:n.3060+24A=
ENST00000645953.1:c.*90+3219T= (CCNH) ENSP00000494460.1:n.*90+3219T=
ENST00000646883.1:c.254+3219T= (CCNH)
ENST00000274376.10:c.3060+24A= (RASA1) ENSP00000274376.6:n.3060+24A=
ENST00000456692.6:c.2529+24A= (RASA1) ENSP00000411221.2:n.2529+24A=
ENST00000506290.1:c.2562+24A= (RASA1) ENSP00000420905.1:n.2562+24A=
ENST00000512763.5:c.2559+24A= (RASA1) ENSP00000422008.1:n.2559+24A=
ENST00000515800.6:c.*1675+24A= (RASA1) ENSP00000423395.2:n.*1675+24A=
NM_002890.2:c.3060+24A= (RASA1) NP_002881.1:n.3060+24A=
NM_022650.2:c.2529+24A= (RASA1) NP_072179.1:n.2529+24A=
XM_011543525.1:c.2973+24A= (RASA1) XP_011541827.1:n.2973+24A=
NM_001364075.1:c.933+5493T= (CCNH) NP_001351004.1:n.933+5493T=
NR_157068.1:n.1447+3219T= (CCNH)
NR_157069.1:n.1040+3219T= (CCNH)
NR_157070.1:n.1204+3219T= (CCNH)
XM_011543525.2:c.2973+24A= (RASA1) XP_011541827.1:n.2973+24A=
NM_001364075.2:c.933+5493T= (CCNH) NP_001351004.1:n.933+5493T=
NM_002890.3:c.3060+24A= (RASA1) MANE Select NP_002881.1:n.3060+24A=
NR_157068.2:n.1447+3219T= (CCNH)
NR_157069.2:n.1040+3219T= (CCNH)
NR_157070.2:n.1204+3219T= (CCNH)
NM_022650.3:c.2529+24A= (RASA1) NP_072179.1:n.2529+24A=