Canonical Allele Identifier: CA445402381
Gene: RASA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.86564715C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268898C>A , CM000667.2:g.87268898C>A GRCh38
NC_000005.9:g.86564715C>A , CM000667.1:g.86564715C>A GRCh37
NC_000005.8:g.86600471C>A NCBI36
NG_011650.1:g.5565C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.447C>A MANE Select ENSP00000274376.6:p.Gly149=
ENST00000274376.10:c.447C>A ENSP00000274376.6:p.Gly149=
ENST00000515800.6:c.447C>A ENSP00000423395.2:p.Gly149=
NM_002890.2:c.447C>A NP_002881.1:p.Gly149=
XM_011543525.1:c.447C>A XP_011541827.1:p.Gly149=
XM_011543526.1:c.447C>A XP_011541828.1:p.Gly149=
XM_011543527.1:c.447C>A XP_011541829.1:p.Gly149=
XM_011543525.2:c.447C>A XP_011541827.1:p.Gly149=
XM_011543527.3:c.447C>A XP_011541829.1:p.Gly149=
NM_002890.3:c.447C>A MANE Select NP_002881.1:p.Gly149=