Canonical Allele Identifier: CA3335442
Gene: RASA1 HGNC NCBI

Linked Data

dbSNP Id: rs780636400
gnomAD v4: 5-87268923-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268923T>A , CM000667.2:g.87268923T>A GRCh38
NC_000005.9:g.86564740T>A , CM000667.1:g.86564740T>A GRCh37
NC_000005.8:g.86600496T>A NCBI36
NG_011650.1:g.5590T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.472T>A MANE Select ENSP00000274376.6:p.Ser158Thr
ENST00000274376.10:c.472T>A ENSP00000274376.6:p.Ser158Thr
ENST00000515800.6:c.472T>A ENSP00000423395.2:p.Ser158Thr
NM_002890.2:c.472T>A NP_002881.1:p.Ser158Thr
XM_011543525.1:c.472T>A XP_011541827.1:p.Ser158Thr
XM_011543526.1:c.472T>A XP_011541828.1:p.Ser158Thr
XM_011543527.1:c.472T>A XP_011541829.1:p.Ser158Thr
XM_011543525.2:c.472T>A XP_011541827.1:p.Ser158Thr
XM_011543527.3:c.472T>A XP_011541829.1:p.Ser158Thr
NM_002890.3:c.472T>A MANE Select NP_002881.1:p.Ser158Thr