Canonical Allele Identifier: CA2168427895

Gene: ARHGAP11A-SCG5 ARHGAP11A

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32635275C>G , CM000677.2:g.32635275C>G	GRCh38
NC_000015.9:g.32927476C>G , CM000677.1:g.32927476C>G	GRCh37
NC_000015.8:g.30714768C>G	NCBI36
NG_051557.1:g.26543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689909.1:c.1229+2167C>G (ARHGAP11A-SCG5)	ENSP00000510704.1:n.1229+2167C>G
ENST00000692248.1:c.1235+2167C>G (ARHGAP11A-SCG5)	ENSP00000510771.1:n.1235+2167C>G
ENST00000361627.8:c.1345-502C>G (ARHGAP11A) MANE Select	ENSP00000355090.3:n.1345-502C>G
ENST00000361627.7:c.1345-502C>G (ARHGAP11A)	ENSP00000355090.3:n.1345-502C>G
ENST00000543522.5:c.778-502C>G (ARHGAP11A)	ENSP00000440073.1:n.778-502C>G
ENST00000562481.1:c.396-502C>G (ARHGAP11A)
ENST00000563864.5:c.1261-502C>G (ARHGAP11A)	ENSP00000456078.1:n.1261-502C>G
ENST00000564918.1:n.394-502C>G (ARHGAP11A)
ENST00000565905.5:c.778-502C>G (ARHGAP11A)	ENSP00000455754.1:n.778-502C>G
ENST00000567348.5:c.1345-502C>G (ARHGAP11A)	ENSP00000454575.1:n.1345-502C>G
NM_001286479.1:c.778-502C>G (ARHGAP11A)	NP_001273408.1:n.778-502C>G
NM_001286480.1:c.778-502C>G (ARHGAP11A)	NP_001273409.1:n.778-502C>G
NM_014783.4:c.1345-502C>G (ARHGAP11A)	NP_055598.1:n.1345-502C>G
NM_199357.1:c.1345-502C>G (ARHGAP11A)	NP_955389.1:n.1345-502C>G
XM_005254808.3:c.1258-502C>G (ARHGAP11A)	XP_005254865.1:n.1258-502C>G
XM_011522260.1:c.1345-502C>G (ARHGAP11A)	XP_011520562.1:n.1345-502C>G
XM_011522261.1:c.1261-502C>G (ARHGAP11A)	XP_011520563.1:n.1261-502C>G
XM_011522262.1:c.778-502C>G (ARHGAP11A)	XP_011520564.1:n.778-502C>G
NM_001286479.2:c.778-502C>G (ARHGAP11A)	NP_001273408.1:n.778-502C>G
NM_001286480.2:c.778-502C>G (ARHGAP11A)	NP_001273409.1:n.778-502C>G
NM_014783.5:c.1345-502C>G (ARHGAP11A)	NP_055598.1:n.1345-502C>G
NM_199357.2:c.1345-502C>G (ARHGAP11A)	NP_955389.1:n.1345-502C>G
NM_014783.6:c.1345-502C>G (ARHGAP11A) MANE Select	NP_055598.1:n.1345-502C>G
NM_001286480.3:c.778-502C>G (ARHGAP11A)	NP_001273409.1:n.778-502C>G
NM_001368319.1:c.1235+2167C>G (ARHGAP11A-SCG5)	NP_001355248.1:n.1235+2167C>G
NM_001286479.3:c.778-502C>G (ARHGAP11A)	NP_001273408.1:n.778-502C>G
NM_199357.3:c.1345-502C>G (ARHGAP11A)	NP_955389.1:n.1345-502C>G