Canonical Allele Identifier: CA453648389

Gene: RAC1

Linked Data

• dbSNP Id: rs770760616
• gnomAD v2: 7-6431666-G-T
• gnomAD v4: 7-6392035-G-T
• MyVariant Identifiers: chr7:g.6431666G>T (hg19) ; chr7:g.6392035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392035G>T , CM000669.2:g.6392035G>T	GRCh38
NC_000007.13:g.6431666G>T , CM000669.1:g.6431666G>T	GRCh37
NC_000007.12:g.6398191G>T	NCBI36
NG_029431.1:g.22541G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.407G>T
ENST00000704002.1:c.318G>T	ENSP00000515615.1:p.Pro106=
ENST00000704003.1:c.*172G>T	ENSP00000515616.1:n.*172G>T
ENST00000348035.9:c.219G>T MANE Select	ENSP00000258737.7:p.Pro73=
ENST00000348035.8:c.219G>T	ENSP00000258737.7:p.Pro73=
ENST00000356142.4:c.219G>T	ENSP00000348461.4:p.Pro73=
ENST00000488373.5:n.450G>T
ENST00000497741.5:n.235G>T
NM_006908.4:c.219G>T	NP_008839.2:p.Pro73=
NM_018890.3:c.219G>T	NP_061485.1:p.Pro73=
NM_006908.5:c.219G>T MANE Select	NP_008839.2:p.Pro73=
NM_018890.4:c.219G>T	NP_061485.1:p.Pro73=