Canonical Allele Identifier: CA366761397

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431646T>G (hg19) ; chr7:g.6392015T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392015T>G , CM000669.2:g.6392015T>G	GRCh38
NC_000007.13:g.6431646T>G , CM000669.1:g.6431646T>G	GRCh37
NC_000007.12:g.6398171T>G	NCBI36
NG_029431.1:g.22521T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.387T>G
ENST00000704002.1:c.298T>G	ENSP00000515615.1:p.Leu100Val
ENST00000704003.1:c.*152T>G	ENSP00000515616.1:n.*152T>G
ENST00000348035.9:c.199T>G MANE Select	ENSP00000258737.7:p.Leu67Val
ENST00000348035.8:c.199T>G	ENSP00000258737.7:p.Leu67Val
ENST00000356142.4:c.199T>G	ENSP00000348461.4:p.Leu67Val
ENST00000488373.5:n.430T>G
ENST00000497741.5:n.215T>G
NM_006908.4:c.199T>G	NP_008839.2:p.Leu67Val
NM_018890.3:c.199T>G	NP_061485.1:p.Leu67Val
NM_006908.5:c.199T>G MANE Select	NP_008839.2:p.Leu67Val
NM_018890.4:c.199T>G	NP_061485.1:p.Leu67Val