Canonical Allele Identifier: CA1561615256

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87389330_87389339delinsTCAAAAAAAA , CM000667.2:g.87389330_87389339delinsTCAAAAAAAA GRCh38
NC_000005.9:g.86685147_86685156delinsTCAAAAAAAA , CM000667.1:g.86685147_86685156delinsTCAAAAAAAA GRCh37
NC_000005.8:g.86720903_86720912delinsTCAAAAAAAA NCBI36
NG_011650.1:g.125997_126006delinsTCAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.2926-63_2926-54delinsTCAAAAAAAA (RASA1) MANE Select ENSP00000274376.6:n.2926-63_2926-54delinsTCAAAAAAAA
ENST00000645953.1:c.*90+3431_*90+3440delinsTTTTTTTTGA (CCNH) ENSP00000494460.1:n.*90+3431_*90+3440delinsTTTTTTTTGA
ENST00000646883.1:c.254+3431_254+3440delinsTTTTTTTTGA (CCNH)
ENST00000274376.10:c.2926-63_2926-54delinsTCAAAAAAAA (RASA1) ENSP00000274376.6:n.2926-63_2926-54delinsTCAAAAAAAA
ENST00000456692.6:c.2395-63_2395-54delinsTCAAAAAAAA (RASA1) ENSP00000411221.2:n.2395-63_2395-54delinsTCAAAAAAAA
ENST00000506290.1:c.2428-63_2428-54delinsTCAAAAAAAA (RASA1) ENSP00000420905.1:n.2428-63_2428-54delinsTCAAAAAAAA
ENST00000512763.5:c.2425-63_2425-54delinsTCAAAAAAAA (RASA1) ENSP00000422008.1:n.2425-63_2425-54delinsTCAAAAAAAA
ENST00000515800.6:c.*1478_*1487delinsTCAAAAAAAA (RASA1) ENSP00000423395.2:n.*1478_*1487delinsTCAAAAAAAA
NM_002890.2:c.2926-63_2926-54delinsTCAAAAAAAA (RASA1) NP_002881.1:n.2926-63_2926-54delinsTCAAAAAAAA
NM_022650.2:c.2395-63_2395-54delinsTCAAAAAAAA (RASA1) NP_072179.1:n.2395-63_2395-54delinsTCAAAAAAAA
XM_011543525.1:c.2839-63_2839-54delinsTCAAAAAAAA (RASA1) XP_011541827.1:n.2839-63_2839-54delinsTCAAAAAAAA
NM_001364075.1:c.933+5705_933+5714delinsTTTTTTTTGA (CCNH) NP_001351004.1:n.933+5705_933+5714delinsTTTTTTTTGA
NR_157068.1:n.1447+3431_1447+3440delinsTTTTTTTTGA (CCNH)
NR_157069.1:n.1040+3431_1040+3440delinsTTTTTTTTGA (CCNH)
NR_157070.1:n.1204+3431_1204+3440delinsTTTTTTTTGA (CCNH)
XM_011543525.2:c.2839-63_2839-54delinsTCAAAAAAAA (RASA1) XP_011541827.1:n.2839-63_2839-54delinsTCAAAAAAAA
NM_001364075.2:c.933+5705_933+5714delinsTTTTTTTTGA (CCNH) NP_001351004.1:n.933+5705_933+5714delinsTTTTTTTTGA
NM_002890.3:c.2926-63_2926-54delinsTCAAAAAAAA (RASA1) MANE Select NP_002881.1:n.2926-63_2926-54delinsTCAAAAAAAA
NR_157068.2:n.1447+3431_1447+3440delinsTTTTTTTTGA (CCNH)
NR_157069.2:n.1040+3431_1040+3440delinsTTTTTTTTGA (CCNH)
NR_157070.2:n.1204+3431_1204+3440delinsTTTTTTTTGA (CCNH)
NM_022650.3:c.2395-63_2395-54delinsTCAAAAAAAA (RASA1) NP_072179.1:n.2395-63_2395-54delinsTCAAAAAAAA