Canonical Allele Identifier: CA445402425
Gene: RASA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.86564742T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268925T>G , CM000667.2:g.87268925T>G GRCh38
NC_000005.9:g.86564742T>G , CM000667.1:g.86564742T>G GRCh37
NC_000005.8:g.86600498T>G NCBI36
NG_011650.1:g.5592T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.474T>G MANE Select ENSP00000274376.6:p.Ser158=
ENST00000274376.10:c.474T>G ENSP00000274376.6:p.Ser158=
ENST00000515800.6:c.474T>G ENSP00000423395.2:p.Ser158=
NM_002890.2:c.474T>G NP_002881.1:p.Ser158=
NM_022650.2:c.-123T>G NP_072179.1:n.-123T>G
XM_011543525.1:c.474T>G XP_011541827.1:p.Ser158=
XM_011543526.1:c.474T>G XP_011541828.1:p.Ser158=
XM_011543527.1:c.474T>G XP_011541829.1:p.Ser158=
XM_011543525.2:c.474T>G XP_011541827.1:p.Ser158=
XM_011543527.3:c.474T>G XP_011541829.1:p.Ser158=
NM_002890.3:c.474T>G MANE Select NP_002881.1:p.Ser158=