Canonical Allele Identifier: CA8375528

Gene: ARHGEF15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8320860C>A , CM000679.2:g.8320860C>A	GRCh38
NC_000017.10:g.8224178C>A , CM000679.1:g.8224178C>A	GRCh37
NC_000017.9:g.8164903C>A	NCBI36
NG_034063.1:g.15623C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361926.8:c.2393C>A MANE Select	ENSP00000355026.3:p.Pro798His
ENST00000647883.1:c.1856C>A	ENSP00000498197.1:p.Pro619His
ENST00000361926.7:c.2393C>A	ENSP00000355026.3:p.Pro798His
ENST00000421050.2:c.2393C>A	ENSP00000412505.1:p.Pro798His
NM_025014.1:c.2393C>A	NP_079290.1:p.Pro798His
NM_173728.3:c.2393C>A	NP_776089.2:p.Pro798His
XM_011523734.1:c.2438C>A	XP_011522036.1:p.Pro813His
XM_011523735.1:c.2438C>A	XP_011522037.1:p.Pro813His
XM_011523736.1:c.*10C>A	XP_011522038.1:n.*10C>A
XM_011523737.1:c.1187C>A	XP_011522039.1:p.Pro396His
XM_011523734.2:c.2438C>A	XP_011522036.1:p.Pro813His
XM_011523736.2:c.*10C>A	XP_011522038.1:n.*10C>A
NM_173728.4:c.2393C>A MANE Select	NP_776089.2:p.Pro798His
NM_025014.2:c.2393C>A	NP_079290.1:p.Pro798His