Canonical Allele Identifier: CA2674514787

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331339_87331340dup , CM000667.2:g.87331339_87331340dup GRCh38
NC_000005.9:g.86627156_86627157dup , CM000667.1:g.86627156_86627157dup GRCh37
NC_000005.8:g.86662912_86662913dup NCBI36
NG_011650.1:g.68006_68007dup

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.540-9_540-8dup (RASA1) MANE Select ENSP00000274376.6:n.540-9_540-8dup
ENST00000645953.1:c.*91-12440_*91-12439dup (CCNH) ENSP00000494460.1:n.*91-12440_*91-12439du...
ENST00000274376.10:c.540-9_540-8dup (RASA1) ENSP00000274376.6:n.540-9_540-8dup
ENST00000456692.6:c.9-9_9-8dup (RASA1) ENSP00000411221.2:n.9-9_9-8dup
ENST00000506290.1:c.42-9_42-8dup (RASA1) ENSP00000420905.1:n.42-9_42-8dup
ENST00000512763.5:c.39-9_39-8dup (RASA1) ENSP00000422008.1:n.39-9_39-8dup
ENST00000515800.6:c.540-9_540-8dup (RASA1) ENSP00000423395.2:n.540-9_540-8dup
NM_002890.2:c.540-9_540-8dup (RASA1) NP_002881.1:n.540-9_540-8dup
NM_022650.2:c.9-9_9-8dup (RASA1) NP_072179.1:n.9-9_9-8dup
XM_011543525.1:c.540-9_540-8dup (RASA1) XP_011541827.1:n.540-9_540-8dup
XM_011543526.1:c.540-9_540-8dup (RASA1) XP_011541828.1:n.540-9_540-8dup
XM_011543527.1:c.540-9_540-8dup (RASA1) XP_011541829.1:n.540-9_540-8dup
NM_001364075.1:c.934-18542_934-18541dup (CCNH) NP_001351004.1:n.934-18542_934-18541dup
NR_157068.1:n.1448-18542_1448-18541dup (CCNH)
NR_157069.1:n.1041-18542_1041-18541dup (CCNH)
NR_157070.1:n.1205-18542_1205-18541dup (CCNH)
XM_011543525.2:c.540-9_540-8dup (RASA1) XP_011541827.1:n.540-9_540-8dup
XM_011543527.3:c.540-9_540-8dup (RASA1) XP_011541829.1:n.540-9_540-8dup
NM_001364075.2:c.934-18542_934-18541dup (CCNH) NP_001351004.1:n.934-18542_934-18541dup
NM_002890.3:c.540-9_540-8dup (RASA1) MANE Select NP_002881.1:n.540-9_540-8dup
NR_157068.2:n.1448-18542_1448-18541dup (CCNH)
NR_157069.2:n.1041-18542_1041-18541dup (CCNH)
NR_157070.2:n.1205-18542_1205-18541dup (CCNH)
NM_022650.3:c.9-9_9-8dup (RASA1) NP_072179.1:n.9-9_9-8dup