Canonical Allele Identifier: CA453648100

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431624T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391993T>C , CM000669.2:g.6391993T>C	GRCh38
NC_000007.13:g.6431624T>C , CM000669.1:g.6431624T>C	GRCh37
NC_000007.12:g.6398149T>C	NCBI36
NG_029431.1:g.22499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.365T>C
ENST00000704002.1:c.276T>C	ENSP00000515615.1:p.Ala92=
ENST00000704003.1:c.*130T>C	ENSP00000515616.1:n.*130T>C
ENST00000348035.9:c.177T>C MANE Select	ENSP00000258737.7:p.Ala59=
ENST00000348035.8:c.177T>C	ENSP00000258737.7:p.Ala59=
ENST00000356142.4:c.177T>C	ENSP00000348461.4:p.Ala59=
ENST00000488373.5:n.408T>C
ENST00000497741.5:n.193T>C
NM_006908.4:c.177T>C	NP_008839.2:p.Ala59=
NM_018890.3:c.177T>C	NP_061485.1:p.Ala59=
NM_006908.5:c.177T>C MANE Select	NP_008839.2:p.Ala59=
NM_018890.4:c.177T>C	NP_061485.1:p.Ala59=