Canonical Allele Identifier: CA2339183432
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003913_47003923delinsGACACGCACAC , CM000681.2:g.47003913_47003923delinsGACACGCACAC GRCh38
NC_000019.9:g.47507170_47507180delinsGACACGCACAC , CM000681.1:g.47507170_47507180delinsGACACGCACAC GRCh37
NC_000019.8:g.52199010_52199020delinsGACACGCACAC NCBI36
NG_047014.1:g.90347_90357delinsGACACGCACAC
NG_047014.2:g.147917_147927delinsGACACGCACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7725_7735delinsGACACGCACAC ENSP00000385720.2:n.7725_7735delinsGACACGCACAC
ENST00000672722.1:c.*3225_*3235delinsGACACGCACAC MANE Select ENSP00000500409.1:n.*3225_*3235delinsGACACGCACAC
ENST00000404338.7:c.7725_7735delinsGACACGCACAC ENSP00000385720.2:n.7725_7735delinsGACACGCACAC
ENST00000614079.1:c.7302_7312delinsGACACGCACAC ENSP00000483730.1:n.7302_7312delinsGACACGCACAC
NM_004491.4:c.7725_7735delinsGACACGCACAC NP_004482.4:n.7725_7735delinsGACACGCACAC
NM_004491.5:c.*3225_*3235delinsGACACGCACAC MANE Select NP_004482.4:n.*3225_*3235delinsGACACGCACAC
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