Canonical Allele Identifier: CA2573158134
Community Standard Title: NM_002872.5(RAC2):c.288+10A>G
Gene: RAC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37231922T>C , CM000684.2:g.37231922T>C GRCh38
NC_000022.10:g.37627962T>C , CM000684.1:g.37627962T>C GRCh37
NC_000022.9:g.35957908T>C NCBI36
NG_007288.1:g.17344A>G , LRG_97:g.17344A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002872.5:c.288+10A>G MANE Select NP_002863.1:n.288+10A>G
ENST00000249071.11:c.288+10A>G MANE Select ENSP00000249071.6:n.288+10A>G
NM_002872.4:c.288+10A>G NP_002863.1:n.288+10A>G
ENST00000249071.10:c.288+10A>G ENSP00000249071.6:n.288+10A>G
ENST00000405484.5:c.267+10A>G ENSP00000385590.1:n.267+10A>G
ENST00000406508.5:c.156+10A>G ENSP00000385270.1:n.156+10A>G
ENST00000441619.5:c.288+10A>G ENSP00000403778.1:n.288+10A>G
ENST00000699915.1:n.346+10A>G
XM_006724286.2:c.288+10A>G XP_006724349.1:n.288+10A>G
XM_006724286.3:c.288+10A>G XP_006724349.1:n.288+10A>G