Canonical Allele Identifier: CA1294396007

Gene: ARHGAP15

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.143338658_143338659delinsCT , CM000664.2:g.143338658_143338659delinsCT	GRCh38
NC_000002.11:g.144096227_144096228delinsCT , CM000664.1:g.144096227_144096228delinsCT	GRCh37
NC_000002.10:g.143812697_143812698delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295095.11:c.474+88058_474+88059delinsCT MANE Select	ENSP00000295095.6:n.474+88058_474+88059delinsCT
ENST00000295095.10:c.474+88058_474+88059delinsCT	ENSP00000295095.6:n.474+88058_474+88059delinsCT
ENST00000460776.5:n.422+88058_422+88059delinsCT
ENST00000469117.5:n.205+88058_205+88059delinsCT
ENST00000474474.5:n.238+88058_238+88059delinsCT
ENST00000552641.5:n.542+88058_542+88059delinsCT
NM_018460.3:c.474+88058_474+88059delinsCT	NP_060930.3:n.474+88058_474+88059delinsCT
XM_006712632.2:c.474+88058_474+88059delinsCT	XP_006712695.1:n.474+88058_474+88059delinsCT
XM_011511479.1:c.474+88058_474+88059delinsCT	XP_011509781.1:n.474+88058_474+88059delinsCT
XM_011511480.1:c.474+88058_474+88059delinsCT	XP_011509782.1:n.474+88058_474+88059delinsCT
XM_011511481.1:c.474+88058_474+88059delinsCT	XP_011509783.1:n.474+88058_474+88059delinsCT
XM_011511482.1:c.474+88058_474+88059delinsCT	XP_011509784.1:n.474+88058_474+88059delinsCT
XM_011511483.1:c.240+88058_240+88059delinsCT	XP_011509785.1:n.240+88058_240+88059delinsCT
XM_011511484.1:c.474+88058_474+88059delinsCT	XP_011509786.1:n.474+88058_474+88059delinsCT
XM_011511479.2:c.474+88058_474+88059delinsCT	XP_011509781.1:n.474+88058_474+88059delinsCT
XM_011511481.2:c.474+88058_474+88059delinsCT	XP_011509783.1:n.474+88058_474+88059delinsCT
XM_011511482.2:c.474+88058_474+88059delinsCT	XP_011509784.1:n.474+88058_474+88059delinsCT
XM_017004499.2:c.474+88058_474+88059delinsCT	XP_016859988.1:n.474+88058_474+88059delinsCT
XM_017004500.2:c.345+88058_345+88059delinsCT	XP_016859989.1:n.345+88058_345+88059delinsCT
XM_017004501.1:c.474+88058_474+88059delinsCT	XP_016859990.1:n.474+88058_474+88059delinsCT
XR_001738850.1:n.560+88058_560+88059delinsCT
NM_018460.4:c.474+88058_474+88059delinsCT MANE Select	NP_060930.3:n.474+88058_474+88059delinsCT