Canonical Allele Identifier: CA916669534

Gene: ARHGAP15

Linked Data

• dbSNP Id: rs1558904282

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.143338601_143338607del , CM000664.2:g.143338601_143338607del	GRCh38
NC_000002.11:g.144096170_144096176del , CM000664.1:g.144096170_144096176del	GRCh37
NC_000002.10:g.143812640_143812646del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295095.11:c.474+88001_474+88007del MANE Select	ENSP00000295095.6:n.474+88001_474+88007del
ENST00000295095.10:c.474+88001_474+88007del	ENSP00000295095.6:n.474+88001_474+88007del
ENST00000460776.5:n.422+88001_422+88007del
ENST00000469117.5:n.205+88001_205+88007del
ENST00000474474.5:n.238+88001_238+88007del
ENST00000552641.5:n.542+88001_542+88007del
NM_018460.3:c.474+88001_474+88007del	NP_060930.3:n.474+88001_474+88007del
XM_006712632.2:c.474+88001_474+88007del	XP_006712695.1:n.474+88001_474+88007del
XM_011511479.1:c.474+88001_474+88007del	XP_011509781.1:n.474+88001_474+88007del
XM_011511480.1:c.474+88001_474+88007del	XP_011509782.1:n.474+88001_474+88007del
XM_011511481.1:c.474+88001_474+88007del	XP_011509783.1:n.474+88001_474+88007del
XM_011511482.1:c.474+88001_474+88007del	XP_011509784.1:n.474+88001_474+88007del
XM_011511483.1:c.240+88001_240+88007del	XP_011509785.1:n.240+88001_240+88007del
XM_011511484.1:c.474+88001_474+88007del	XP_011509786.1:n.474+88001_474+88007del
XM_011511479.2:c.474+88001_474+88007del	XP_011509781.1:n.474+88001_474+88007del
XM_011511481.2:c.474+88001_474+88007del	XP_011509783.1:n.474+88001_474+88007del
XM_011511482.2:c.474+88001_474+88007del	XP_011509784.1:n.474+88001_474+88007del
XM_017004499.2:c.474+88001_474+88007del	XP_016859988.1:n.474+88001_474+88007del
XM_017004500.2:c.345+88001_345+88007del	XP_016859989.1:n.345+88001_345+88007del
XM_017004501.1:c.474+88001_474+88007del	XP_016859990.1:n.474+88001_474+88007del
XR_001738850.1:n.560+88001_560+88007del
NM_018460.4:c.474+88001_474+88007del MANE Select	NP_060930.3:n.474+88001_474+88007del