Canonical Allele Identifier: CA366760785

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431578T>A (hg19) ; chr7:g.6391947T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391947T>A , CM000669.2:g.6391947T>A	GRCh38
NC_000007.13:g.6431578T>A , CM000669.1:g.6431578T>A	GRCh37
NC_000007.12:g.6398103T>A	NCBI36
NG_029431.1:g.22453T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.319T>A
ENST00000704002.1:c.230T>A	ENSP00000515615.1:p.Val77Asp
ENST00000704003.1:c.*84T>A	ENSP00000515616.1:n.*84T>A
ENST00000348035.9:c.131T>A MANE Select	ENSP00000258737.7:p.Val44Asp
ENST00000348035.8:c.131T>A	ENSP00000258737.7:p.Val44Asp
ENST00000356142.4:c.131T>A	ENSP00000348461.4:p.Val44Asp
ENST00000488373.5:n.362T>A
ENST00000497741.5:n.147T>A
NM_006908.4:c.131T>A	NP_008839.2:p.Val44Asp
NM_018890.3:c.131T>A	NP_061485.1:p.Val44Asp
NM_006908.5:c.131T>A MANE Select	NP_008839.2:p.Val44Asp
NM_018890.4:c.131T>A	NP_061485.1:p.Val44Asp