Canonical Allele Identifier: CA360374884

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87374272A>T , CM000667.2:g.87374272A>T	GRCh38
NC_000005.9:g.86670089A>T , CM000667.1:g.86670089A>T	GRCh37
NC_000005.8:g.86705845A>T	NCBI36
NG_011650.1:g.110939A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.1886A>T (RASA1) MANE Select	ENSP00000274376.6:p.His629Leu
ENST00000645953.1:c.*90+18498T>A (CCNH)	ENSP00000494460.1:n.*90+18498T>A
ENST00000274376.10:c.1886A>T (RASA1)	ENSP00000274376.6:p.His629Leu
ENST00000456692.6:c.1355A>T (RASA1)	ENSP00000411221.2:p.His452Leu
ENST00000506290.1:c.1388A>T (RASA1)	ENSP00000420905.1:p.His463Leu
ENST00000512763.5:c.1385A>T (RASA1)	ENSP00000422008.1:p.His462Leu
ENST00000515800.6:c.*411A>T (RASA1)	ENSP00000423395.2:n.*411A>T
NM_002890.2:c.1886A>T (RASA1)	NP_002881.1:p.His629Leu
NM_022650.2:c.1355A>T (RASA1)	NP_072179.1:p.His452Leu
XM_011543525.1:c.1886A>T (RASA1)	XP_011541827.1:p.His629Leu
XM_011543526.1:c.1886A>T (RASA1)	XP_011541828.1:p.His629Leu
XR_948544.1:n.743-584T>A
NM_001364075.1:c.933+20772T>A (CCNH)	NP_001351004.1:n.933+20772T>A
NR_157068.1:n.1447+18498T>A (CCNH)
NR_157069.1:n.1040+18498T>A (CCNH)
NR_157070.1:n.1204+18498T>A (CCNH)
XM_011543525.2:c.1886A>T (RASA1)	XP_011541827.1:p.His629Leu
NM_001364075.2:c.933+20772T>A (CCNH)	NP_001351004.1:n.933+20772T>A
NM_002890.3:c.1886A>T (RASA1) MANE Select	NP_002881.1:p.His629Leu
NR_157068.2:n.1447+18498T>A (CCNH)
NR_157069.2:n.1040+18498T>A (CCNH)
NR_157070.2:n.1204+18498T>A (CCNH)
NM_022650.3:c.1355A>T (RASA1)	NP_072179.1:p.His452Leu