Canonical Allele Identifier: CA561260883
Gene: RASA1 HGNC NCBI

Linked Data

dbSNP Id: rs1202633266

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87269013del , CM000667.2:g.87269013del GRCh38
NC_000005.9:g.86564830del , CM000667.1:g.86564830del GRCh37
NC_000005.8:g.86600586del NCBI36
NG_011650.1:g.5680del

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.539+23del MANE Select ENSP00000274376.6:n.539+23del
ENST00000274376.10:c.539+23del ENSP00000274376.6:n.539+23del
ENST00000456692.6:c.-35del ENSP00000411221.2:n.-35del
ENST00000506290.1:c.-48del ENSP00000420905.1:n.-48del
ENST00000512763.5:c.-132del ENSP00000422008.1:n.-132del
ENST00000515800.6:c.539+23del ENSP00000423395.2:n.539+23del
NM_002890.2:c.539+23del NP_002881.1:n.539+23del
NM_022650.2:c.-35del NP_072179.1:n.-35del
XM_011543525.1:c.539+23del XP_011541827.1:n.539+23del
XM_011543526.1:c.539+23del XP_011541828.1:n.539+23del
XM_011543527.1:c.539+23del XP_011541829.1:n.539+23del
XM_011543525.2:c.539+23del XP_011541827.1:n.539+23del
XM_011543527.3:c.539+23del XP_011541829.1:n.539+23del
NM_002890.3:c.539+23del MANE Select NP_002881.1:n.539+23del
NM_022650.3:c.-35del NP_072179.1:n.-35del