Canonical Allele Identifier: CA445402380

Gene: RASA1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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