Canonical Allele Identifier: CA645562937

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87389414_87389415insG , CM000667.2:g.87389414_87389415insG GRCh38
NC_000005.9:g.86685231_86685232insG , CM000667.1:g.86685231_86685232insG GRCh37
NC_000005.8:g.86720987_86720988insG NCBI36
NG_011650.1:g.126081_126082insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.2947_2948insG (RASA1) MANE Select ENSP00000274376.6:p.Thr983SerfsTer6
ENST00000645953.1:c.*90+3355_*90+3356insC (CCNH) ENSP00000494460.1:n.*90+3355_*90+3356insC
ENST00000646883.1:c.254+3355_254+3356insC (CCNH)
ENST00000274376.10:c.2947_2948insG (RASA1) ENSP00000274376.6:p.Thr983SerfsTer6
ENST00000456692.6:c.2416_2417insG (RASA1) ENSP00000411221.2:p.Thr806SerfsTer6
ENST00000506290.1:c.2449_2450insG (RASA1) ENSP00000420905.1:p.Thr817SerfsTer6
ENST00000512763.5:c.2446_2447insG (RASA1) ENSP00000422008.1:p.Thr816SerfsTer6
ENST00000515800.6:c.*1562_*1563insG (RASA1) ENSP00000423395.2:n.*1562_*1563insG
NM_002890.2:c.2947_2948insG (RASA1) NP_002881.1:p.Thr983SerfsTer6
NM_022650.2:c.2416_2417insG (RASA1) NP_072179.1:p.Thr806SerfsTer6
XM_011543525.1:c.2860_2861insG (RASA1) XP_011541827.1:p.Thr954SerfsTer6
NM_001364075.1:c.933+5629_933+5630insC (CCNH) NP_001351004.1:n.933+5629_933+5630insC
NR_157068.1:n.1447+3355_1447+3356insC (CCNH)
NR_157069.1:n.1040+3355_1040+3356insC (CCNH)
NR_157070.1:n.1204+3355_1204+3356insC (CCNH)
XM_011543525.2:c.2860_2861insG (RASA1) XP_011541827.1:p.Thr954SerfsTer6
NM_001364075.2:c.933+5629_933+5630insC (CCNH) NP_001351004.1:n.933+5629_933+5630insC
NM_002890.3:c.2947_2948insG (RASA1) MANE Select NP_002881.1:p.Thr983SerfsTer6
NR_157068.2:n.1447+3355_1447+3356insC (CCNH)
NR_157069.2:n.1040+3355_1040+3356insC (CCNH)
NR_157070.2:n.1204+3355_1204+3356insC (CCNH)
NM_022650.3:c.2416_2417insG (RASA1) NP_072179.1:p.Thr806SerfsTer6