Canonical Allele Identifier: CA11085608
Gene: ARHGAP15 HGNC NCBI

Linked Data

dbSNP Id: rs13428598

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.143492918C>T , CM000664.2:g.143492918C>T GRCh38
NC_000002.11:g.144250487C>T , CM000664.1:g.144250487C>T GRCh37
NC_000002.10:g.143966957C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295095.11:c.826+5423C>T MANE Select ENSP00000295095.6:n.826+5423C>T
ENST00000295095.10:c.826+5423C>T ENSP00000295095.6:n.826+5423C>T
ENST00000548242.5:n.376+5423C>T
ENST00000552289.1:n.133+5423C>T
NM_018460.3:c.826+5423C>T NP_060930.3:n.826+5423C>T
XM_005263714.1:c.124+5423C>T XP_005263771.1:n.124+5423C>T
XM_006712632.2:c.826+5423C>T XP_006712695.1:n.826+5423C>T
XM_011511479.1:c.826+5423C>T XP_011509781.1:n.826+5423C>T
XM_011511480.1:c.826+5423C>T XP_011509782.1:n.826+5423C>T
XM_011511481.1:c.826+5423C>T XP_011509783.1:n.826+5423C>T
XM_011511482.1:c.826+5423C>T XP_011509784.1:n.826+5423C>T
XM_011511483.1:c.592+5423C>T XP_011509785.1:n.592+5423C>T
XM_011511484.1:c.826+5423C>T XP_011509786.1:n.826+5423C>T
XM_011511479.2:c.826+5423C>T XP_011509781.1:n.826+5423C>T
XM_011511481.2:c.826+5423C>T XP_011509783.1:n.826+5423C>T
XM_011511482.2:c.826+5423C>T XP_011509784.1:n.826+5423C>T
XM_017004499.2:c.826+5423C>T XP_016859988.1:n.826+5423C>T
XM_017004500.2:c.697+5423C>T XP_016859989.1:n.697+5423C>T
XM_017004501.1:c.826+5423C>T XP_016859990.1:n.826+5423C>T
XM_024453000.1:c.124+5423C>T XP_024308768.1:n.124+5423C>T
XM_024453001.1:c.124+5423C>T XP_024308769.1:n.124+5423C>T
XR_001738850.1:n.912+5423C>T
NM_018460.4:c.826+5423C>T MANE Select NP_060930.3:n.826+5423C>T