Canonical Allele Identifier: CA2339183483
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003951_47003956delinsAAACTT , CM000681.2:g.47003951_47003956delinsAAACTT GRCh38
NC_000019.9:g.47507208_47507213delinsAAACTT , CM000681.1:g.47507208_47507213delinsAAACTT GRCh37
NC_000019.8:g.52199048_52199053delinsAAACTT NCBI36
NG_047014.1:g.90385_90390delinsAAACTT
NG_047014.2:g.147955_147960delinsAAACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7763_7768delinsAAACTT ENSP00000385720.2:n.7763_7768delinsAAACTT
ENST00000672722.1:c.*3263_*3268delinsAAACTT MANE Select ENSP00000500409.1:n.*3263_*3268delinsAAACTT
ENST00000404338.7:c.7763_7768delinsAAACTT ENSP00000385720.2:n.7763_7768delinsAAACTT
ENST00000614079.1:c.7340_7345delinsAAACTT ENSP00000483730.1:n.7340_7345delinsAAACTT
NM_004491.4:c.7763_7768delinsAAACTT NP_004482.4:n.7763_7768delinsAAACTT
NM_004491.5:c.*3263_*3268delinsAAACTT MANE Select NP_004482.4:n.*3263_*3268delinsAAACTT