Canonical Allele Identifier: CA1561579903

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87333207_87333208delinsCT , CM000667.2:g.87333207_87333208delinsCT	GRCh38
NC_000005.9:g.86629024_86629025delinsCT , CM000667.1:g.86629024_86629025delinsCT	GRCh37
NC_000005.8:g.86664780_86664781delinsCT	NCBI36
NG_011650.1:g.69874_69875delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.829-60_829-59delinsCT (RASA1) MANE Select	ENSP00000274376.6:n.829-60_829-59delinsCT
ENST00000645953.1:c.*91-14311_*91-14310delinsAG (CCNH)	ENSP00000494460.1:n.*91-14311_*91-14310delinsAG
ENST00000274376.10:c.829-60_829-59delinsCT (RASA1)	ENSP00000274376.6:n.829-60_829-59delinsCT
ENST00000456692.6:c.298-60_298-59delinsCT (RASA1)	ENSP00000411221.2:n.298-60_298-59delinsCT
ENST00000506290.1:c.331-60_331-59delinsCT (RASA1)	ENSP00000420905.1:n.331-60_331-59delinsCT
ENST00000512763.5:c.328-60_328-59delinsCT (RASA1)	ENSP00000422008.1:n.328-60_328-59delinsCT
ENST00000515800.6:c.829-60_829-59delinsCT (RASA1)	ENSP00000423395.2:n.829-60_829-59delinsCT
NM_002890.2:c.829-60_829-59delinsCT (RASA1)	NP_002881.1:n.829-60_829-59delinsCT
NM_022650.2:c.298-60_298-59delinsCT (RASA1)	NP_072179.1:n.298-60_298-59delinsCT
XM_011543525.1:c.829-60_829-59delinsCT (RASA1)	XP_011541827.1:n.829-60_829-59delinsCT
XM_011543526.1:c.829-60_829-59delinsCT (RASA1)	XP_011541828.1:n.829-60_829-59delinsCT
XM_011543527.1:c.829-60_829-59delinsCT (RASA1)	XP_011541829.1:n.829-60_829-59delinsCT
NM_001364075.1:c.934-20413_934-20412delinsAG (CCNH)	NP_001351004.1:n.934-20413_934-20412delinsAG
NR_157068.1:n.1448-20413_1448-20412delinsAG (CCNH)
NR_157069.1:n.1041-20413_1041-20412delinsAG (CCNH)
NR_157070.1:n.1205-20413_1205-20412delinsAG (CCNH)
XM_011543525.2:c.829-60_829-59delinsCT (RASA1)	XP_011541827.1:n.829-60_829-59delinsCT
XM_011543527.3:c.829-60_829-59delinsCT (RASA1)	XP_011541829.1:n.829-60_829-59delinsCT
NM_001364075.2:c.934-20413_934-20412delinsAG (CCNH)	NP_001351004.1:n.934-20413_934-20412delinsAG
NM_002890.3:c.829-60_829-59delinsCT (RASA1) MANE Select	NP_002881.1:n.829-60_829-59delinsCT
NR_157068.2:n.1448-20413_1448-20412delinsAG (CCNH)
NR_157069.2:n.1041-20413_1041-20412delinsAG (CCNH)
NR_157070.2:n.1205-20413_1205-20412delinsAG (CCNH)
NM_022650.3:c.298-60_298-59delinsCT (RASA1)	NP_072179.1:n.298-60_298-59delinsCT