Canonical Allele Identifier: CA153350704

Gene: RAC1

Linked Data

• dbSNP Id: rs528566314
• gnomAD v2: 7-6431861-G-C
• gnomAD v3: 7-6392230-G-C
• gnomAD v4: 7-6392230-G-C
• MyVariant Identifiers: chr7:g.6431861G>C (hg19) ; chr7:g.6392230G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392230G>C , CM000669.2:g.6392230G>C	GRCh38
NC_000007.13:g.6431861G>C , CM000669.1:g.6431861G>C	GRCh37
NC_000007.12:g.6398386G>C	NCBI36
NG_029431.1:g.22736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.602G>C
ENST00000704002.1:c.324+189G>C	ENSP00000515615.1:n.324+189G>C
ENST00000704003.1:c.*178+189G>C	ENSP00000515616.1:n.*178+189G>C
ENST00000348035.9:c.225+189G>C MANE Select	ENSP00000258737.7:n.225+189G>C
ENST00000348035.8:c.225+189G>C	ENSP00000258737.7:n.225+189G>C
ENST00000356142.4:c.225+189G>C	ENSP00000348461.4:n.225+189G>C
ENST00000488373.5:n.456+189G>C
ENST00000497741.5:n.241+189G>C
NM_006908.4:c.225+189G>C	NP_008839.2:n.225+189G>C
NM_018890.3:c.225+189G>C	NP_061485.1:n.225+189G>C
NM_006908.5:c.225+189G>C MANE Select	NP_008839.2:n.225+189G>C
NM_018890.4:c.225+189G>C	NP_061485.1:n.225+189G>C