Canonical Allele Identifier: CA360387987

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86685228G>T (hg19) ; chr5:g.87389411G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389411G>T , CM000667.2:g.87389411G>T	GRCh38
NC_000005.9:g.86685228G>T , CM000667.1:g.86685228G>T	GRCh37
NC_000005.8:g.86720984G>T	NCBI36
NG_011650.1:g.126078G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2944G>T (RASA1) MANE Select	ENSP00000274376.6:p.Asp982Tyr
ENST00000645953.1:c.*90+3359C>A (CCNH)	ENSP00000494460.1:n.*90+3359C>A
ENST00000646883.1:c.254+3359C>A (CCNH)
ENST00000274376.10:c.2944G>T (RASA1)	ENSP00000274376.6:p.Asp982Tyr
ENST00000456692.6:c.2413G>T (RASA1)	ENSP00000411221.2:p.Asp805Tyr
ENST00000506290.1:c.2446G>T (RASA1)	ENSP00000420905.1:p.Asp816Tyr
ENST00000512763.5:c.2443G>T (RASA1)	ENSP00000422008.1:p.Asp815Tyr
ENST00000515800.6:c.*1559G>T (RASA1)	ENSP00000423395.2:n.*1559G>T
NM_002890.2:c.2944G>T (RASA1)	NP_002881.1:p.Asp982Tyr
NM_022650.2:c.2413G>T (RASA1)	NP_072179.1:p.Asp805Tyr
XM_011543525.1:c.2857G>T (RASA1)	XP_011541827.1:p.Asp953Tyr
NM_001364075.1:c.933+5633C>A (CCNH)	NP_001351004.1:n.933+5633C>A
NR_157068.1:n.1447+3359C>A (CCNH)
NR_157069.1:n.1040+3359C>A (CCNH)
NR_157070.1:n.1204+3359C>A (CCNH)
XM_011543525.2:c.2857G>T (RASA1)	XP_011541827.1:p.Asp953Tyr
NM_001364075.2:c.933+5633C>A (CCNH)	NP_001351004.1:n.933+5633C>A
NM_002890.3:c.2944G>T (RASA1) MANE Select	NP_002881.1:p.Asp982Tyr
NR_157068.2:n.1447+3359C>A (CCNH)
NR_157069.2:n.1040+3359C>A (CCNH)
NR_157070.2:n.1204+3359C>A (CCNH)
NM_022650.3:c.2413G>T (RASA1)	NP_072179.1:p.Asp805Tyr