Canonical Allele Identifier: CA360365204

Linked Data

gnomAD v4: 5-87353215-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87353215A>G , CM000667.2:g.87353215A>G GRCh38
NC_000005.9:g.86649032A>G , CM000667.1:g.86649032A>G GRCh37
NC_000005.8:g.86684788A>G NCBI36
NG_011650.1:g.89882A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.1312A>G (RASA1) MANE Select ENSP00000274376.6:p.Lys438Glu
ENST00000645953.1:c.*91-34318T>C (CCNH) ENSP00000494460.1:n.*91-34318T>C
ENST00000274376.10:c.1312A>G (RASA1) ENSP00000274376.6:p.Lys438Glu
ENST00000456692.6:c.781A>G (RASA1) ENSP00000411221.2:p.Lys261Glu
ENST00000506290.1:c.814A>G (RASA1) ENSP00000420905.1:p.Lys272Glu
ENST00000509953.1:n.415A>G (RASA1)
ENST00000512763.5:c.811A>G (RASA1) ENSP00000422008.1:p.Lys271Glu
ENST00000515800.6:c.1312A>G (RASA1) ENSP00000423395.2:p.Lys438Glu
NM_002890.2:c.1312A>G (RASA1) NP_002881.1:p.Lys438Glu
NM_022650.2:c.781A>G (RASA1) NP_072179.1:p.Lys261Glu
XM_011543525.1:c.1312A>G (RASA1) XP_011541827.1:p.Lys438Glu
XM_011543526.1:c.1312A>G (RASA1) XP_011541828.1:p.Lys438Glu
XM_011543527.1:c.1312A>G (RASA1) XP_011541829.1:p.Lys438Glu
NM_001364075.1:c.934-40420T>C (CCNH) NP_001351004.1:n.934-40420T>C
NR_157068.1:n.1447+39555T>C (CCNH)
NR_157069.1:n.1040+39555T>C (CCNH)
NR_157070.1:n.1204+39555T>C (CCNH)
XM_011543525.2:c.1312A>G (RASA1) XP_011541827.1:p.Lys438Glu
XM_011543527.3:c.1312A>G (RASA1) XP_011541829.1:p.Lys438Glu
NM_001364075.2:c.934-40420T>C (CCNH) NP_001351004.1:n.934-40420T>C
NM_002890.3:c.1312A>G (RASA1) MANE Select NP_002881.1:p.Lys438Glu
NR_157068.2:n.1447+39555T>C (CCNH)
NR_157069.2:n.1040+39555T>C (CCNH)
NR_157070.2:n.1204+39555T>C (CCNH)
NM_022650.3:c.781A>G (RASA1) NP_072179.1:p.Lys261Glu