Canonical Allele Identifier: CA560888452

Gene: RASA1 CCNH

Linked Data

• dbSNP Id: rs1328929185
• gnomAD v2: 5-86627328-A-AATTTG
• MyVariant Identifiers: chr5:g.86627328_86627329insATTTG (hg19) ; chr5:g.87331511_87331512insATTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331511_87331512insATTTG , CM000667.2:g.87331511_87331512insATTTG	GRCh38
NC_000005.9:g.86627328_86627329insATTTG , CM000667.1:g.86627328_86627329insATTTG	GRCh37
NC_000005.8:g.86663084_86663085insATTTG	NCBI36
NG_011650.1:g.68178_68179insATTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.692+11_692+12insATTTG (RASA1) MANE Select	ENSP00000274376.6:n.692+11_692+12insATTTG
ENST00000645953.1:c.*91-12615_*91-12614insCAAAT (CCNH)	ENSP00000494460.1:n.*91-12615_*91-12614insCAAAT
ENST00000274376.10:c.692+11_692+12insATTTG (RASA1)	ENSP00000274376.6:n.692+11_692+12insATTTG
ENST00000456692.6:c.161+11_161+12insATTTG (RASA1)	ENSP00000411221.2:n.161+11_161+12insATTTG
ENST00000506290.1:c.194+11_194+12insATTTG (RASA1)	ENSP00000420905.1:n.194+11_194+12insATTTG
ENST00000512763.5:c.191+11_191+12insATTTG (RASA1)	ENSP00000422008.1:n.191+11_191+12insATTTG
ENST00000515800.6:c.692+11_692+12insATTTG (RASA1)	ENSP00000423395.2:n.692+11_692+12insATTTG
NM_002890.2:c.692+11_692+12insATTTG (RASA1)	NP_002881.1:n.692+11_692+12insATTTG
NM_022650.2:c.161+11_161+12insATTTG (RASA1)	NP_072179.1:n.161+11_161+12insATTTG
XM_011543525.1:c.692+11_692+12insATTTG (RASA1)	XP_011541827.1:n.692+11_692+12insATTTG
XM_011543526.1:c.692+11_692+12insATTTG (RASA1)	XP_011541828.1:n.692+11_692+12insATTTG
XM_011543527.1:c.692+11_692+12insATTTG (RASA1)	XP_011541829.1:n.692+11_692+12insATTTG
NM_001364075.1:c.934-18717_934-18716insCAAAT (CCNH)	NP_001351004.1:n.934-18717_934-18716insCAAAT
NR_157068.1:n.1448-18717_1448-18716insCAAAT (CCNH)
NR_157069.1:n.1041-18717_1041-18716insCAAAT (CCNH)
NR_157070.1:n.1205-18717_1205-18716insCAAAT (CCNH)
XM_011543525.2:c.692+11_692+12insATTTG (RASA1)	XP_011541827.1:n.692+11_692+12insATTTG
XM_011543527.3:c.692+11_692+12insATTTG (RASA1)	XP_011541829.1:n.692+11_692+12insATTTG
NM_001364075.2:c.934-18717_934-18716insCAAAT (CCNH)	NP_001351004.1:n.934-18717_934-18716insCAAAT
NM_002890.3:c.692+11_692+12insATTTG (RASA1) MANE Select	NP_002881.1:n.692+11_692+12insATTTG
NR_157068.2:n.1448-18717_1448-18716insCAAAT (CCNH)
NR_157069.2:n.1041-18717_1041-18716insCAAAT (CCNH)
NR_157070.2:n.1205-18717_1205-18716insCAAAT (CCNH)
NM_022650.3:c.161+11_161+12insATTTG (RASA1)	NP_072179.1:n.161+11_161+12insATTTG