Canonical Allele Identifier: CA2404246531
Community Standard Title: NM_002872.5(RAC2):c.169G= (p.Asp57=)
Gene: RAC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37232857C= , CM000684.2:g.37232857C= GRCh38
NC_000022.10:g.37628897C= , CM000684.1:g.37628897C= GRCh37
NC_000022.9:g.35958843C= NCBI36
NG_007288.1:g.16409G= , LRG_97:g.16409G=

Transcript Alleles

HGVS Amino-acid Change
NM_002872.5:c.169G= MANE Select NP_002863.1:p.Asp57=
ENST00000249071.11:c.169G= MANE Select ENSP00000249071.6:p.Asp57=
NM_002872.4:c.169G= NP_002863.1:p.Asp57=
ENST00000249071.10:c.169G= ENSP00000249071.6:p.Asp57=
ENST00000405484.5:c.148G= ENSP00000385590.1:p.Asp50=
ENST00000406508.5:c.37G= ENSP00000385270.1:p.Asp13=
ENST00000441619.5:c.169G= ENSP00000403778.1:p.Asp57=
ENST00000469532.1:n.299G=
ENST00000699915.1:n.227G=
XM_006724286.2:c.169G= XP_006724349.1:p.Asp57=
XM_006724286.3:c.169G= XP_006724349.1:p.Asp57=