Canonical Allele Identifier: CA2339183669
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004262_47004268delinsAGGAAGG , CM000681.2:g.47004262_47004268delinsAGGAAGG GRCh38
NC_000019.9:g.47507519_47507525delinsAGGAAGG , CM000681.1:g.47507519_47507525delinsAGGAAGG GRCh37
NC_000019.8:g.52199359_52199365delinsAGGAAGG NCBI36
NG_047014.1:g.90696_90702delinsAGGAAGG
NG_047014.2:g.148266_148272delinsAGGAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8074_8080delinsAGGAAGG ENSP00000385720.2:n.8074_8080delinsAGGAAGG
ENST00000672722.1:c.*3574_*3580delinsAGGAAGG MANE Select ENSP00000500409.1:n.*3574_*3580delinsAGGAAGG
ENST00000404338.7:c.8074_8080delinsAGGAAGG ENSP00000385720.2:n.8074_8080delinsAGGAAGG
ENST00000614079.1:c.7651_7657delinsAGGAAGG ENSP00000483730.1:n.7651_7657delinsAGGAAGG
NM_004491.4:c.8074_8080delinsAGGAAGG NP_004482.4:n.8074_8080delinsAGGAAGG
NM_004491.5:c.*3574_*3580delinsAGGAAGG MANE Select NP_004482.4:n.*3574_*3580delinsAGGAAGG