Canonical Allele Identifier: CA445402385
Gene: RASA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.86564718C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268901C>A , CM000667.2:g.87268901C>A GRCh38
NC_000005.9:g.86564718C>A , CM000667.1:g.86564718C>A GRCh37
NC_000005.8:g.86600474C>A NCBI36
NG_011650.1:g.5568C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.450C>A MANE Select ENSP00000274376.6:p.Leu150=
ENST00000274376.10:c.450C>A ENSP00000274376.6:p.Leu150=
ENST00000515800.6:c.450C>A ENSP00000423395.2:p.Leu150=
NM_002890.2:c.450C>A NP_002881.1:p.Leu150=
XM_011543525.1:c.450C>A XP_011541827.1:p.Leu150=
XM_011543526.1:c.450C>A XP_011541828.1:p.Leu150=
XM_011543527.1:c.450C>A XP_011541829.1:p.Leu150=
XM_011543525.2:c.450C>A XP_011541827.1:p.Leu150=
XM_011543527.3:c.450C>A XP_011541829.1:p.Leu150=
NM_002890.3:c.450C>A MANE Select NP_002881.1:p.Leu150=