Canonical Allele Identifier: CA1561615392

Gene: RASA1 CCNH

Linked Data

• dbSNP Id: rs1762302561
• gnomAD v4: 5-87389348-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389350_87389351del , CM000667.2:g.87389350_87389351del	GRCh38
NC_000005.9:g.86685167_86685168del , CM000667.1:g.86685167_86685168del	GRCh37
NC_000005.8:g.86720923_86720924del	NCBI36
NG_011650.1:g.126017_126018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2926-43_2926-42del (RASA1) MANE Select	ENSP00000274376.6:n.2926-43_2926-42del
ENST00000645953.1:c.*90+3420_*90+3421del (CCNH)	ENSP00000494460.1:n.*90+3420_*90+3421del
ENST00000646883.1:c.254+3420_254+3421del (CCNH)
ENST00000274376.10:c.2926-43_2926-42del (RASA1)	ENSP00000274376.6:n.2926-43_2926-42del
ENST00000456692.6:c.2395-43_2395-42del (RASA1)	ENSP00000411221.2:n.2395-43_2395-42del
ENST00000506290.1:c.2428-43_2428-42del (RASA1)	ENSP00000420905.1:n.2428-43_2428-42del
ENST00000512763.5:c.2425-43_2425-42del (RASA1)	ENSP00000422008.1:n.2425-43_2425-42del
ENST00000515800.6:c.*1498_*1499del (RASA1)	ENSP00000423395.2:n.*1498_*1499del
NM_002890.2:c.2926-43_2926-42del (RASA1)	NP_002881.1:n.2926-43_2926-42del
NM_022650.2:c.2395-43_2395-42del (RASA1)	NP_072179.1:n.2395-43_2395-42del
XM_011543525.1:c.2839-43_2839-42del (RASA1)	XP_011541827.1:n.2839-43_2839-42del
NM_001364075.1:c.933+5694_933+5695del (CCNH)	NP_001351004.1:n.933+5694_933+5695del
NR_157068.1:n.1447+3420_1447+3421del (CCNH)
NR_157069.1:n.1040+3420_1040+3421del (CCNH)
NR_157070.1:n.1204+3420_1204+3421del (CCNH)
XM_011543525.2:c.2839-43_2839-42del (RASA1)	XP_011541827.1:n.2839-43_2839-42del
NM_001364075.2:c.933+5694_933+5695del (CCNH)	NP_001351004.1:n.933+5694_933+5695del
NM_002890.3:c.2926-43_2926-42del (RASA1) MANE Select	NP_002881.1:n.2926-43_2926-42del
NR_157068.2:n.1447+3420_1447+3421del (CCNH)
NR_157069.2:n.1040+3420_1040+3421del (CCNH)
NR_157070.2:n.1204+3420_1204+3421del (CCNH)
NM_022650.3:c.2395-43_2395-42del (RASA1)	NP_072179.1:n.2395-43_2395-42del