Canonical Allele Identifier: CA360376550

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331493C>T , CM000667.2:g.87331493C>T GRCh38
NC_000005.9:g.86627310C>T , CM000667.1:g.86627310C>T GRCh37
NC_000005.8:g.86663066C>T NCBI36
NG_011650.1:g.68160C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.685C>T (RASA1) MANE Select ENSP00000274376.6:p.His229Tyr
ENST00000645953.1:c.*91-12596G>A (CCNH) ENSP00000494460.1:n.*91-12596G>A
ENST00000274376.10:c.685C>T (RASA1) ENSP00000274376.6:p.His229Tyr
ENST00000456692.6:c.154C>T (RASA1) ENSP00000411221.2:p.His52Tyr
ENST00000506290.1:c.187C>T (RASA1) ENSP00000420905.1:p.His63Tyr
ENST00000512763.5:c.184C>T (RASA1) ENSP00000422008.1:p.His62Tyr
ENST00000515800.6:c.685C>T (RASA1) ENSP00000423395.2:p.His229Tyr
NM_002890.2:c.685C>T (RASA1) NP_002881.1:p.His229Tyr
NM_022650.2:c.154C>T (RASA1) NP_072179.1:p.His52Tyr
XM_011543525.1:c.685C>T (RASA1) XP_011541827.1:p.His229Tyr
XM_011543526.1:c.685C>T (RASA1) XP_011541828.1:p.His229Tyr
XM_011543527.1:c.685C>T (RASA1) XP_011541829.1:p.His229Tyr
NM_001364075.1:c.934-18698G>A (CCNH) NP_001351004.1:n.934-18698G>A
NR_157068.1:n.1448-18698G>A (CCNH)
NR_157069.1:n.1041-18698G>A (CCNH)
NR_157070.1:n.1205-18698G>A (CCNH)
XM_011543525.2:c.685C>T (RASA1) XP_011541827.1:p.His229Tyr
XM_011543527.3:c.685C>T (RASA1) XP_011541829.1:p.His229Tyr
NM_001364075.2:c.934-18698G>A (CCNH) NP_001351004.1:n.934-18698G>A
NM_002890.3:c.685C>T (RASA1) MANE Select NP_002881.1:p.His229Tyr
NR_157068.2:n.1448-18698G>A (CCNH)
NR_157069.2:n.1041-18698G>A (CCNH)
NR_157070.2:n.1205-18698G>A (CCNH)
NM_022650.3:c.154C>T (RASA1) NP_072179.1:p.His52Tyr