Canonical Allele Identifier: CA453648213

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431642C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392011C>T , CM000669.2:g.6392011C>T	GRCh38
NC_000007.13:g.6431642C>T , CM000669.1:g.6431642C>T	GRCh37
NC_000007.12:g.6398167C>T	NCBI36
NG_029431.1:g.22517C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.383C>T
ENST00000704002.1:c.294C>T	ENSP00000515615.1:p.Asp98=
ENST00000704003.1:c.*148C>T	ENSP00000515616.1:n.*148C>T
ENST00000348035.9:c.195C>T MANE Select	ENSP00000258737.7:p.Asp65=
ENST00000348035.8:c.195C>T	ENSP00000258737.7:p.Asp65=
ENST00000356142.4:c.195C>T	ENSP00000348461.4:p.Asp65=
ENST00000488373.5:n.426C>T
ENST00000497741.5:n.211C>T
NM_006908.4:c.195C>T	NP_008839.2:p.Asp65=
NM_018890.3:c.195C>T	NP_061485.1:p.Asp65=
NM_006908.5:c.195C>T MANE Select	NP_008839.2:p.Asp65=
NM_018890.4:c.195C>T	NP_061485.1:p.Asp65=