Canonical Allele Identifier: CA366760749

Gene: RAC1

Linked Data

• MyVariant Identifiers: chr7:g.6431571G>T (hg19) ; chr7:g.6391940G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391940G>T , CM000669.2:g.6391940G>T	GRCh38
NC_000007.13:g.6431571G>T , CM000669.1:g.6431571G>T	GRCh37
NC_000007.12:g.6398096G>T	NCBI36
NG_029431.1:g.22446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.312G>T
ENST00000704002.1:c.223G>T	ENSP00000515615.1:p.Ala75Ser
ENST00000704003.1:c.*77G>T	ENSP00000515616.1:n.*77G>T
ENST00000348035.9:c.124G>T MANE Select	ENSP00000258737.7:p.Ala42Ser
ENST00000348035.8:c.124G>T	ENSP00000258737.7:p.Ala42Ser
ENST00000356142.4:c.124G>T	ENSP00000348461.4:p.Ala42Ser
ENST00000488373.5:n.355G>T
ENST00000497741.5:n.140G>T
NM_006908.4:c.124G>T	NP_008839.2:p.Ala42Ser
NM_018890.3:c.124G>T	NP_061485.1:p.Ala42Ser
NM_006908.5:c.124G>T MANE Select	NP_008839.2:p.Ala42Ser
NM_018890.4:c.124G>T	NP_061485.1:p.Ala42Ser