Canonical Allele Identifier: CA2614978675

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722196-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722204_72722205del , CM000673.2:g.72722204_72722205del	GRCh38
NC_000011.9:g.72433249_72433250del , CM000673.1:g.72433249_72433250del	GRCh37
NC_000011.8:g.72110897_72110898del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4422_509+4423del MANE Select	ENSP00000377233.3:n.509+4422_509+4423del
ENST00000334211.12:c.-575_-574del	ENSP00000335506.8:n.-575_-574del
ENST00000359373.9:c.509+4422_509+4423del	ENSP00000352332.5:n.509+4422_509+4423del
ENST00000393609.7:c.509+4422_509+4423del	ENSP00000377233.3:n.509+4422_509+4423del
NM_001040118.2:c.509+4422_509+4423del	NP_001035207.1:n.509+4422_509+4423del
NM_001135190.1:c.-575_-574del	NP_001128662.1:n.-575_-574del
NM_015242.4:c.-575_-574del	NP_056057.2:n.-575_-574del
NM_001369489.1:c.-575_-574del	NP_001356418.1:n.-575_-574del
NR_161388.1:n.143_144del
NM_001040118.3:c.509+4422_509+4423del MANE Select	NP_001035207.1:n.509+4422_509+4423del
NM_001135190.2:c.-575_-574del	NP_001128662.1:n.-575_-574del
NM_015242.5:c.-575_-574del	NP_056057.2:n.-575_-574del