Canonical Allele Identifier: CA2580094944

Gene: ARHGEF15

Linked Data

• ClinVar Variation Id: 2020832
• ClinVar RCV Id: RCV002857575

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8312261_8312262delinsAA , CM000679.2:g.8312261_8312262delinsAA	GRCh38
NC_000017.10:g.8215579_8215580delinsAA , CM000679.1:g.8215579_8215580delinsAA	GRCh37
NC_000017.9:g.8156304_8156305delinsAA	NCBI36
NG_034063.1:g.7024_7025delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361926.8:c.222_223delinsAA MANE Select	ENSP00000355026.3:p.Leu75Ile
ENST00000361926.7:c.222_223delinsAA	ENSP00000355026.3:p.Leu75Ile
ENST00000421050.2:c.222_223delinsAA	ENSP00000412505.1:p.Leu75Ile
ENST00000455564.3:n.335_336delinsAA
ENST00000579439.5:c.222_223delinsAA	ENSP00000464540.1:p.Leu75Ile
ENST00000583529.1:c.222_223delinsAA	ENSP00000462796.1:p.Leu75Ile
NM_025014.1:c.222_223delinsAA	NP_079290.1:p.Leu75Ile
NM_173728.3:c.222_223delinsAA	NP_776089.2:p.Leu75Ile
XM_011523734.1:c.222_223delinsAA	XP_011522036.1:p.Leu75Ile
XM_011523735.1:c.222_223delinsAA	XP_011522037.1:p.Leu75Ile
XM_011523736.1:c.222_223delinsAA	XP_011522038.1:p.Leu75Ile
XM_011523734.2:c.222_223delinsAA	XP_011522036.1:p.Leu75Ile
XM_011523736.2:c.222_223delinsAA	XP_011522038.1:p.Leu75Ile
NM_173728.4:c.222_223delinsAA MANE Select	NP_776089.2:p.Leu75Ile
NM_025014.2:c.222_223delinsAA	NP_079290.1:p.Leu75Ile