Canonical Allele Identifier: CA2674518821

Gene: RASA1 CCNH

Linked Data

• gnomAD v4: 5-87389337-AAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389340_87389342del , CM000667.2:g.87389340_87389342del	GRCh38
NC_000005.9:g.86685157_86685159del , CM000667.1:g.86685157_86685159del	GRCh37
NC_000005.8:g.86720913_86720915del	NCBI36
NG_011650.1:g.126007_126009del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2926-53_2926-51del (RASA1) MANE Select	ENSP00000274376.6:n.2926-53_2926-51del
ENST00000645953.1:c.*90+3430_*90+3432del (CCNH)	ENSP00000494460.1:n.*90+3430_*90+3432del
ENST00000646883.1:c.254+3430_254+3432del (CCNH)
ENST00000274376.10:c.2926-53_2926-51del (RASA1)	ENSP00000274376.6:n.2926-53_2926-51del
ENST00000456692.6:c.2395-53_2395-51del (RASA1)	ENSP00000411221.2:n.2395-53_2395-51del
ENST00000506290.1:c.2428-53_2428-51del (RASA1)	ENSP00000420905.1:n.2428-53_2428-51del
ENST00000512763.5:c.2425-53_2425-51del (RASA1)	ENSP00000422008.1:n.2425-53_2425-51del
ENST00000515800.6:c.*1488_*1490del (RASA1)	ENSP00000423395.2:n.*1488_*1490del
NM_002890.2:c.2926-53_2926-51del (RASA1)	NP_002881.1:n.2926-53_2926-51del
NM_022650.2:c.2395-53_2395-51del (RASA1)	NP_072179.1:n.2395-53_2395-51del
XM_011543525.1:c.2839-53_2839-51del (RASA1)	XP_011541827.1:n.2839-53_2839-51del
NM_001364075.1:c.933+5704_933+5706del (CCNH)	NP_001351004.1:n.933+5704_933+5706del
NR_157068.1:n.1447+3430_1447+3432del (CCNH)
NR_157069.1:n.1040+3430_1040+3432del (CCNH)
NR_157070.1:n.1204+3430_1204+3432del (CCNH)
XM_011543525.2:c.2839-53_2839-51del (RASA1)	XP_011541827.1:n.2839-53_2839-51del
NM_001364075.2:c.933+5704_933+5706del (CCNH)	NP_001351004.1:n.933+5704_933+5706del
NM_002890.3:c.2926-53_2926-51del (RASA1) MANE Select	NP_002881.1:n.2926-53_2926-51del
NR_157068.2:n.1447+3430_1447+3432del (CCNH)
NR_157069.2:n.1040+3430_1040+3432del (CCNH)
NR_157070.2:n.1204+3430_1204+3432del (CCNH)
NM_022650.3:c.2395-53_2395-51del (RASA1)	NP_072179.1:n.2395-53_2395-51del