Canonical Allele Identifier: CA2674515986

Gene: RASA1 CCNH

Linked Data

• gnomAD v4: 5-87353226-A-ACAGGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87353227_87353228insAGGTTC , CM000667.2:g.87353227_87353228insAGGTTC	GRCh38
NC_000005.9:g.86649044_86649045insAGGTTC , CM000667.1:g.86649044_86649045insAGGTTC	GRCh37
NC_000005.8:g.86684800_86684801insAGGTTC	NCBI36
NG_011650.1:g.89894_89895insAGGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.1324_1325insAGGTTC (RASA1) MANE Select	ENSP00000274376.6:p.Val441_Pro442insGlnVal
ENST00000645953.1:c.*91-34330_*91-34329insAACCTG (CCNH)	ENSP00000494460.1:n.*91-34330_*91-34329insAACCTG
ENST00000274376.10:c.1324_1325insAGGTTC (RASA1)	ENSP00000274376.6:p.Val441_Pro442insGlnVal
ENST00000456692.6:c.793_794insAGGTTC (RASA1)	ENSP00000411221.2:p.Val264_Pro265insGlnVal
ENST00000506290.1:c.826_827insAGGTTC (RASA1)	ENSP00000420905.1:p.Val275_Pro276insGlnVal
ENST00000509953.1:n.427_428insAGGTTC (RASA1)
ENST00000512763.5:c.823_824insAGGTTC (RASA1)	ENSP00000422008.1:p.Val274_Pro275insGlnVal
ENST00000515800.6:c.1324_1325insAGGTTC (RASA1)	ENSP00000423395.2:p.Val441_Pro442insGlnVal
NM_002890.2:c.1324_1325insAGGTTC (RASA1)	NP_002881.1:p.Val441_Pro442insGlnVal
NM_022650.2:c.793_794insAGGTTC (RASA1)	NP_072179.1:p.Val264_Pro265insGlnVal
XM_011543525.1:c.1324_1325insAGGTTC (RASA1)	XP_011541827.1:p.Val441_Pro442insGlnVal
XM_011543526.1:c.1324_1325insAGGTTC (RASA1)	XP_011541828.1:p.Val441_Pro442insGlnVal
XM_011543527.1:c.1324_1325insAGGTTC (RASA1)	XP_011541829.1:p.Val441_Pro442insGlnVal
NM_001364075.1:c.934-40432_934-40431insAACCTG (CCNH)	NP_001351004.1:n.934-40432_934-40431insAACCTG
NR_157068.1:n.1447+39543_1447+39544insAACCTG (CCNH)
NR_157069.1:n.1040+39543_1040+39544insAACCTG (CCNH)
NR_157070.1:n.1204+39543_1204+39544insAACCTG (CCNH)
XM_011543525.2:c.1324_1325insAGGTTC (RASA1)	XP_011541827.1:p.Val441_Pro442insGlnVal
XM_011543527.3:c.1324_1325insAGGTTC (RASA1)	XP_011541829.1:p.Val441_Pro442insGlnVal
NM_001364075.2:c.934-40432_934-40431insAACCTG (CCNH)	NP_001351004.1:n.934-40432_934-40431insAACCTG
NM_002890.3:c.1324_1325insAGGTTC (RASA1) MANE Select	NP_002881.1:p.Val441_Pro442insGlnVal
NR_157068.2:n.1447+39543_1447+39544insAACCTG (CCNH)
NR_157069.2:n.1040+39543_1040+39544insAACCTG (CCNH)
NR_157070.2:n.1204+39543_1204+39544insAACCTG (CCNH)
NM_022650.3:c.793_794insAGGTTC (RASA1)	NP_072179.1:p.Val264_Pro265insGlnVal