Canonical Allele Identifier: CA536709169

Gene: ARHGAP15

Linked Data

• dbSNP Id: rs1558904352
• gnomAD v2: 2-144096234-T-TAAA
• gnomAD v3: 2-143338665-T-TAAA
• gnomAD v4: 2-143338665-T-TAAA
• MyVariant Identifiers: chr2:g.144096234_144096235insAAA (hg19) ; chr2:g.143338665_143338666insAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.143338665_143338666insAAA , CM000664.2:g.143338665_143338666insAAA	GRCh38
NC_000002.11:g.144096234_144096235insAAA , CM000664.1:g.144096234_144096235insAAA	GRCh37
NC_000002.10:g.143812704_143812705insAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295095.11:c.474+88065_474+88066insAAA MANE Select	ENSP00000295095.6:n.474+88065_474+88066insAAA
ENST00000295095.10:c.474+88065_474+88066insAAA	ENSP00000295095.6:n.474+88065_474+88066insAAA
ENST00000460776.5:n.422+88065_422+88066insAAA
ENST00000469117.5:n.205+88065_205+88066insAAA
ENST00000474474.5:n.238+88065_238+88066insAAA
ENST00000552641.5:n.542+88065_542+88066insAAA
NM_018460.3:c.474+88065_474+88066insAAA	NP_060930.3:n.474+88065_474+88066insAAA
XM_006712632.2:c.474+88065_474+88066insAAA	XP_006712695.1:n.474+88065_474+88066insAAA
XM_011511479.1:c.474+88065_474+88066insAAA	XP_011509781.1:n.474+88065_474+88066insAAA
XM_011511480.1:c.474+88065_474+88066insAAA	XP_011509782.1:n.474+88065_474+88066insAAA
XM_011511481.1:c.474+88065_474+88066insAAA	XP_011509783.1:n.474+88065_474+88066insAAA
XM_011511482.1:c.474+88065_474+88066insAAA	XP_011509784.1:n.474+88065_474+88066insAAA
XM_011511483.1:c.240+88065_240+88066insAAA	XP_011509785.1:n.240+88065_240+88066insAAA
XM_011511484.1:c.474+88065_474+88066insAAA	XP_011509786.1:n.474+88065_474+88066insAAA
XM_011511479.2:c.474+88065_474+88066insAAA	XP_011509781.1:n.474+88065_474+88066insAAA
XM_011511481.2:c.474+88065_474+88066insAAA	XP_011509783.1:n.474+88065_474+88066insAAA
XM_011511482.2:c.474+88065_474+88066insAAA	XP_011509784.1:n.474+88065_474+88066insAAA
XM_017004499.2:c.474+88065_474+88066insAAA	XP_016859988.1:n.474+88065_474+88066insAAA
XM_017004500.2:c.345+88065_345+88066insAAA	XP_016859989.1:n.345+88065_345+88066insAAA
XM_017004501.1:c.474+88065_474+88066insAAA	XP_016859990.1:n.474+88065_474+88066insAAA
XR_001738850.1:n.560+88065_560+88066insAAA
NM_018460.4:c.474+88065_474+88066insAAA MANE Select	NP_060930.3:n.474+88065_474+88066insAAA