Canonical Allele Identifier: CA2339183658

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004241G= , CM000681.2:g.47004241G=	GRCh38
NC_000019.9:g.47507498G= , CM000681.1:g.47507498G=	GRCh37
NC_000019.8:g.52199338G=	NCBI36
NG_047014.1:g.90675G=
NG_047014.2:g.148245G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8053G=	ENSP00000385720.2:n.8053G=
ENST00000672722.1:c.*3553G= MANE Select	ENSP00000500409.1:n.*3553G=
ENST00000404338.7:c.8053G=	ENSP00000385720.2:n.8053G=
ENST00000614079.1:c.7630G=	ENSP00000483730.1:n.7630G=
NM_004491.4:c.8053G=	NP_004482.4:n.8053G=
NM_004491.5:c.*3553G= MANE Select	NP_004482.4:n.*3553G=