Canonical Allele Identifier: CA758166919

Gene: ARHGAP15

Linked Data

• dbSNP Id: rs1182936499
• gnomAD v3: 2-143338803-ATTC-A
• gnomAD v4: 2-143338803-ATTC-A
• MyVariant Identifiers: chr2:g.144096373_144096375del (hg19) ; chr2:g.143338804_143338806del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.143338810_143338812del , CM000664.2:g.143338810_143338812del	GRCh38
NC_000002.11:g.144096379_144096381del , CM000664.1:g.144096379_144096381del	GRCh37
NC_000002.10:g.143812849_143812851del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000295095.11:c.474+88210_474+88212del MANE Select	ENSP00000295095.6:n.474+88210_474+88212de...
ENST00000295095.10:c.474+88210_474+88212del	ENSP00000295095.6:n.474+88210_474+88212de...
ENST00000460776.5:n.422+88210_422+88212del
ENST00000469117.5:n.205+88210_205+88212del
ENST00000474474.5:n.238+88210_238+88212del
ENST00000552641.5:n.542+88210_542+88212del
NM_018460.3:c.474+88210_474+88212del	NP_060930.3:n.474+88210_474+88212del
XM_006712632.2:c.474+88210_474+88212del	XP_006712695.1:n.474+88210_474+88212del
XM_011511479.1:c.474+88210_474+88212del	XP_011509781.1:n.474+88210_474+88212del
XM_011511480.1:c.474+88210_474+88212del	XP_011509782.1:n.474+88210_474+88212del
XM_011511481.1:c.474+88210_474+88212del	XP_011509783.1:n.474+88210_474+88212del
XM_011511482.1:c.474+88210_474+88212del	XP_011509784.1:n.474+88210_474+88212del
XM_011511483.1:c.240+88210_240+88212del	XP_011509785.1:n.240+88210_240+88212del
XM_011511484.1:c.474+88210_474+88212del	XP_011509786.1:n.474+88210_474+88212del
XM_011511479.2:c.474+88210_474+88212del	XP_011509781.1:n.474+88210_474+88212del
XM_011511481.2:c.474+88210_474+88212del	XP_011509783.1:n.474+88210_474+88212del
XM_011511482.2:c.474+88210_474+88212del	XP_011509784.1:n.474+88210_474+88212del
XM_017004499.2:c.474+88210_474+88212del	XP_016859988.1:n.474+88210_474+88212del
XM_017004500.2:c.345+88210_345+88212del	XP_016859989.1:n.345+88210_345+88212del
XM_017004501.1:c.474+88210_474+88212del	XP_016859990.1:n.474+88210_474+88212del
XR_001738850.1:n.560+88210_560+88212del
NM_018460.4:c.474+88210_474+88212del MANE Select	NP_060930.3:n.474+88210_474+88212del