Canonical Allele Identifier: CA366761500

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431652C>T (hg19) ; chr7:g.6392021C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392021C>T , CM000669.2:g.6392021C>T	GRCh38
NC_000007.13:g.6431652C>T , CM000669.1:g.6431652C>T	GRCh37
NC_000007.12:g.6398177C>T	NCBI36
NG_029431.1:g.22527C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.393C>T
ENST00000704002.1:c.304C>T	ENSP00000515615.1:p.Pro102Ser
ENST00000704003.1:c.*158C>T	ENSP00000515616.1:n.*158C>T
ENST00000348035.9:c.205C>T MANE Select	ENSP00000258737.7:p.Pro69Ser
ENST00000348035.8:c.205C>T	ENSP00000258737.7:p.Pro69Ser
ENST00000356142.4:c.205C>T	ENSP00000348461.4:p.Pro69Ser
ENST00000488373.5:n.436C>T
ENST00000497741.5:n.221C>T
NM_006908.4:c.205C>T	NP_008839.2:p.Pro69Ser
NM_018890.3:c.205C>T	NP_061485.1:p.Pro69Ser
NM_006908.5:c.205C>T MANE Select	NP_008839.2:p.Pro69Ser
NM_018890.4:c.205C>T	NP_061485.1:p.Pro69Ser