Canonical Allele Identifier: CA360417309
Gene: RASA1 HGNC NCBI

Linked Data

dbSNP Id: rs1341795065
gnomAD v2: 5-86564662-G-A
gnomAD v4: 5-87268845-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268845G>A , CM000667.2:g.87268845G>A GRCh38
NC_000005.9:g.86564662G>A , CM000667.1:g.86564662G>A GRCh37
NC_000005.8:g.86600418G>A NCBI36
NG_011650.1:g.5512G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.394G>A MANE Select ENSP00000274376.6:p.Gly132Ser
ENST00000274376.10:c.394G>A ENSP00000274376.6:p.Gly132Ser
ENST00000515800.6:c.394G>A ENSP00000423395.2:p.Gly132Ser
NM_002890.2:c.394G>A NP_002881.1:p.Gly132Ser
XM_011543525.1:c.394G>A XP_011541827.1:p.Gly132Ser
XM_011543526.1:c.394G>A XP_011541828.1:p.Gly132Ser
XM_011543527.1:c.394G>A XP_011541829.1:p.Gly132Ser
XM_011543525.2:c.394G>A XP_011541827.1:p.Gly132Ser
XM_011543527.3:c.394G>A XP_011541829.1:p.Gly132Ser
NM_002890.3:c.394G>A MANE Select NP_002881.1:p.Gly132Ser