Canonical Allele Identifier: CA360417192
Gene: RASA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.86564602G>C (hg19) chr5:g.87268785G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268785G>C , CM000667.2:g.87268785G>C GRCh38
NC_000005.9:g.86564602G>C , CM000667.1:g.86564602G>C GRCh37
NC_000005.8:g.86600358G>C NCBI36
NG_011650.1:g.5452G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.334G>C MANE Select ENSP00000274376.6:p.Gly112Arg
ENST00000274376.10:c.334G>C ENSP00000274376.6:p.Gly112Arg
ENST00000515800.6:c.334G>C ENSP00000423395.2:p.Gly112Arg
NM_002890.2:c.334G>C NP_002881.1:p.Gly112Arg
XM_011543525.1:c.334G>C XP_011541827.1:p.Gly112Arg
XM_011543526.1:c.334G>C XP_011541828.1:p.Gly112Arg
XM_011543527.1:c.334G>C XP_011541829.1:p.Gly112Arg
XM_011543525.2:c.334G>C XP_011541827.1:p.Gly112Arg
XM_011543527.3:c.334G>C XP_011541829.1:p.Gly112Arg
NM_002890.3:c.334G>C MANE Select NP_002881.1:p.Gly112Arg
Search 100 bp 5'
Search 100 bp 3'