Canonical Allele Identifier: CA406501236

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46988012C>T , CM000681.2:g.46988012C>T	GRCh38
NC_000019.9:g.47491269C>T , CM000681.1:g.47491269C>T	GRCh37
NC_000019.8:g.52183109C>T	NCBI36
NG_047014.1:g.74446C>T
NG_047014.2:g.132016C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004491.5:c.3850C>T MANE Select	NP_004482.4:p.Arg1284Trp
ENST00000672722.1:c.3850C>T MANE Select	ENSP00000500409.1:p.Arg1284Trp
NM_004491.4:c.3850C>T	NP_004482.4:p.Arg1284Trp
ENST00000404338.7:c.3850C>T	ENSP00000385720.2:p.Arg1284Trp
ENST00000404338.8:c.3850C>T	ENSP00000385720.2:p.Arg1284Trp
ENST00000595822.1:n.113C>T
ENST00000614079.1:c.3850C>T	ENSP00000483730.1:p.Arg1284Trp
ENST00000615647.1:c.2216-12866C>T	ENSP00000479487.1:n.2216-12866C>T
XM_011526873.1:c.3850C>T	XP_011525175.1:p.Arg1284Trp
XM_024451473.1:c.3850C>T	XP_024307241.1:p.Arg1284Trp
XR_002958305.1:n.3959C>T
XR_935811.1:n.3959C>T