Canonical Allele Identifier: CA153350384

Gene: RAC1

Linked Data

• dbSNP Id: rs964265383
• gnomAD v4: 7-6391945-T-C
• MyVariant Identifiers: chr7:g.6431576T>C (hg19) ; chr7:g.6391945T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391945T>C , CM000669.2:g.6391945T>C	GRCh38
NC_000007.13:g.6431576T>C , CM000669.1:g.6431576T>C	GRCh37
NC_000007.12:g.6398101T>C	NCBI36
NG_029431.1:g.22451T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.317T>C
ENST00000704002.1:c.228T>C	ENSP00000515615.1:p.Asn76=
ENST00000704003.1:c.*82T>C	ENSP00000515616.1:n.*82T>C
ENST00000348035.9:c.129T>C MANE Select	ENSP00000258737.7:p.Asn43=
ENST00000348035.8:c.129T>C	ENSP00000258737.7:p.Asn43=
ENST00000356142.4:c.129T>C	ENSP00000348461.4:p.Asn43=
ENST00000488373.5:n.360T>C
ENST00000497741.5:n.145T>C
NM_006908.4:c.129T>C	NP_008839.2:p.Asn43=
NM_018890.3:c.129T>C	NP_061485.1:p.Asn43=
NM_006908.5:c.129T>C MANE Select	NP_008839.2:p.Asn43=
NM_018890.4:c.129T>C	NP_061485.1:p.Asn43=