Canonical Allele Identifier: CA658684005

Gene: ARHGEF15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8313029_8313043del , CM000679.2:g.8313029_8313043del	GRCh38
NC_000017.10:g.8216347_8216361del , CM000679.1:g.8216347_8216361del	GRCh37
NC_000017.9:g.8157072_8157086del	NCBI36
NG_034063.1:g.7792_7806del

Transcript Alleles

HGVS	Amino-acid Change
NM_173728.4:c.709_723del MANE Select	NP_776089.2:p.Val237_Ala241del
ENST00000361926.8:c.709_723del MANE Select	ENSP00000355026.3:p.Val237_Ala241del
NM_025014.1:c.709_723del	NP_079290.1:p.Val237_Ala241del
NM_025014.2:c.709_723del	NP_079290.1:p.Val237_Ala241del
NM_173728.3:c.709_723del	NP_776089.2:p.Val237_Ala241del
ENST00000361926.7:c.709_723del	ENSP00000355026.3:p.Val237_Ala241del
ENST00000421050.2:c.709_723del	ENSP00000412505.1:p.Val237_Ala241del
ENST00000455564.3:n.1103_1117del
XM_011523734.1:c.709_723del	XP_011522036.1:p.Val237_Ala241del
XM_011523734.2:c.709_723del	XP_011522036.1:p.Val237_Ala241del
XM_011523735.1:c.709_723del	XP_011522037.1:p.Val237_Ala241del
XM_011523736.1:c.709_723del	XP_011522038.1:p.Val237_Ala241del
XM_011523736.2:c.709_723del	XP_011522038.1:p.Val237_Ala241del