Canonical Allele Identifier: CA2674518816

Gene: RASA1 CCNH

Linked Data

• gnomAD v4: 5-87389327-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389330_87389331del , CM000667.2:g.87389330_87389331del	GRCh38
NC_000005.9:g.86685147_86685148del , CM000667.1:g.86685147_86685148del	GRCh37
NC_000005.8:g.86720903_86720904del	NCBI36
NG_011650.1:g.125997_125998del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2926-63_2926-62del (RASA1) MANE Select	ENSP00000274376.6:n.2926-63_2926-62del
ENST00000645953.1:c.*90+3441_*90+3442del (CCNH)	ENSP00000494460.1:n.*90+3441_*90+3442del
ENST00000646883.1:c.254+3441_254+3442del (CCNH)
ENST00000274376.10:c.2926-63_2926-62del (RASA1)	ENSP00000274376.6:n.2926-63_2926-62del
ENST00000456692.6:c.2395-63_2395-62del (RASA1)	ENSP00000411221.2:n.2395-63_2395-62del
ENST00000506290.1:c.2428-63_2428-62del (RASA1)	ENSP00000420905.1:n.2428-63_2428-62del
ENST00000512763.5:c.2425-63_2425-62del (RASA1)	ENSP00000422008.1:n.2425-63_2425-62del
ENST00000515800.6:c.*1478_*1479del (RASA1)	ENSP00000423395.2:n.*1478_*1479del
NM_002890.2:c.2926-63_2926-62del (RASA1)	NP_002881.1:n.2926-63_2926-62del
NM_022650.2:c.2395-63_2395-62del (RASA1)	NP_072179.1:n.2395-63_2395-62del
XM_011543525.1:c.2839-63_2839-62del (RASA1)	XP_011541827.1:n.2839-63_2839-62del
NM_001364075.1:c.933+5715_933+5716del (CCNH)	NP_001351004.1:n.933+5715_933+5716del
NR_157068.1:n.1447+3441_1447+3442del (CCNH)
NR_157069.1:n.1040+3441_1040+3442del (CCNH)
NR_157070.1:n.1204+3441_1204+3442del (CCNH)
XM_011543525.2:c.2839-63_2839-62del (RASA1)	XP_011541827.1:n.2839-63_2839-62del
NM_001364075.2:c.933+5715_933+5716del (CCNH)	NP_001351004.1:n.933+5715_933+5716del
NM_002890.3:c.2926-63_2926-62del (RASA1) MANE Select	NP_002881.1:n.2926-63_2926-62del
NR_157068.2:n.1447+3441_1447+3442del (CCNH)
NR_157069.2:n.1040+3441_1040+3442del (CCNH)
NR_157070.2:n.1204+3441_1204+3442del (CCNH)
NM_022650.3:c.2395-63_2395-62del (RASA1)	NP_072179.1:n.2395-63_2395-62del