Canonical Allele Identifier: CA309105971

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46921240C>A , CM000681.2:g.46921240C>A	GRCh38
NC_000019.9:g.47424497C>A , CM000681.1:g.47424497C>A	GRCh37
NC_000019.8:g.52116337C>A	NCBI36
NG_047014.1:g.7674C>A
NG_047014.2:g.65244C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004491.5:c.2565C>A MANE Select	NP_004482.4:p.Tyr855Ter
ENST00000672722.1:c.2565C>A MANE Select	ENSP00000500409.1:p.Tyr855Ter
NM_004491.4:c.2565C>A	NP_004482.4:p.Tyr855Ter
ENST00000404338.7:c.2565C>A	ENSP00000385720.2:p.Tyr855Ter
ENST00000404338.8:c.2565C>A	ENSP00000385720.2:p.Tyr855Ter
ENST00000614079.1:c.2565C>A	ENSP00000483730.1:p.Tyr855Ter
ENST00000615647.1:c.2215+350C>A	ENSP00000479487.1:n.2215+350C>A
ENST00000700035.1:n.458C>A
XM_011526873.1:c.2565C>A	XP_011525175.1:p.Tyr855Ter
XM_024451473.1:c.2565C>A	XP_024307241.1:p.Tyr855Ter
XR_002958305.1:n.2674C>A
XR_935811.1:n.2674C>A