Canonical Allele Identifier: CA2339183410
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003865_47003866delinsAG , CM000681.2:g.47003865_47003866delinsAG GRCh38
NC_000019.9:g.47507122_47507123delinsAG , CM000681.1:g.47507122_47507123delinsAG GRCh37
NC_000019.8:g.52198962_52198963delinsAG NCBI36
NG_047014.1:g.90299_90300delinsAG
NG_047014.2:g.147869_147870delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7677_7678delinsAG ENSP00000385720.2:n.7677_7678delinsAG
ENST00000672722.1:c.*3177_*3178delinsAG MANE Select ENSP00000500409.1:n.*3177_*3178delinsAG
ENST00000404338.7:c.7677_7678delinsAG ENSP00000385720.2:n.7677_7678delinsAG
ENST00000614079.1:c.7254_7255delinsAG ENSP00000483730.1:n.7254_7255delinsAG
NM_004491.4:c.7677_7678delinsAG NP_004482.4:n.7677_7678delinsAG
NM_004491.5:c.*3177_*3178delinsAG MANE Select NP_004482.4:n.*3177_*3178delinsAG