Canonical Allele Identifier: CA2404248158
Community Standard Title: NM_002872.5(RAC2):c.108-3812A=
Gene: RAC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37236730T= , CM000684.2:g.37236730T= GRCh38
NC_000022.10:g.37632770T= , CM000684.1:g.37632770T= GRCh37
NC_000022.9:g.35962716T= NCBI36
NG_007288.1:g.12536A= , LRG_97:g.12536A=

Transcript Alleles

HGVS Amino-acid Change
NM_002872.5:c.108-3812A= MANE Select NP_002863.1:n.108-3812A=
ENST00000249071.11:c.108-3812A= MANE Select ENSP00000249071.6:n.108-3812A=
NM_002872.4:c.108-3812A= NP_002863.1:n.108-3812A=
ENST00000249071.10:c.108-3812A= ENSP00000249071.6:n.108-3812A=
ENST00000405484.5:c.87-3812A= ENSP00000385590.1:n.87-3812A=
ENST00000406508.5:c.-25-3812A= ENSP00000385270.1:n.-25-3812A=
ENST00000441619.5:c.108-3812A= ENSP00000403778.1:n.108-3812A=
ENST00000469532.1:n.238-3812A=
ENST00000699915.1:n.166-3812A=
XM_006724286.2:c.108-3812A= XP_006724349.1:n.108-3812A=
XM_006724286.3:c.108-3812A= XP_006724349.1:n.108-3812A=