Canonical Allele Identifier: CA803919970

Gene: CDC42SE2

Linked Data

• dbSNP Id: rs1301530705
• gnomAD v3: 5-131373848-T-C
• gnomAD v4: 5-131373848-T-C
• MyVariant Identifiers: chr5:g.130709541T>C (hg19) ; chr5:g.131373848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131373848T>C , CM000667.2:g.131373848T>C	GRCh38
NC_000005.9:g.130709541T>C , CM000667.1:g.130709541T>C	GRCh37
NC_000005.8:g.130737440T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505065.2:c.55-11695T>C MANE Select	ENSP00000427421.1:n.55-11695T>C
ENST00000360515.7:c.55-11695T>C	ENSP00000353706.3:n.55-11695T>C
ENST00000395246.5:c.55-11695T>C	ENSP00000378667.1:n.55-11695T>C
ENST00000503291.5:c.-27-11695T>C	ENSP00000426779.1:n.-27-11695T>C
ENST00000505065.1:c.55-11695T>C	ENSP00000427421.1:n.55-11695T>C
NM_001038702.1:c.55-11695T>C	NP_001033791.1:n.55-11695T>C
NM_020240.2:c.55-11695T>C	NP_064625.1:n.55-11695T>C
XM_017009648.2:c.55-11695T>C	XP_016865137.1:n.55-11695T>C
XM_017009649.2:c.55-11695T>C	XP_016865138.1:n.55-11695T>C
NM_001038702.2:c.55-11695T>C	NP_001033791.1:n.55-11695T>C
NM_001375633.1:c.55-11695T>C	NP_001362562.1:n.55-11695T>C
NM_001375634.1:c.55-11695T>C	NP_001362563.1:n.55-11695T>C
NM_001375635.1:c.55-11695T>C MANE Select	NP_001362564.1:n.55-11695T>C
NM_020240.3:c.55-11695T>C	NP_064625.1:n.55-11695T>C