Canonical Allele Identifier: CA2614978614

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722184-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722185_72722186insGG , CM000673.2:g.72722185_72722186insGG	GRCh38
NC_000011.9:g.72433230_72433231insGG , CM000673.1:g.72433230_72433231insGG	GRCh37
NC_000011.8:g.72110878_72110879insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4435_509+4436insCC MANE Select	ENSP00000377233.3:n.509+4435_509+4436insCC
ENST00000334211.12:c.-562_-561insCC	ENSP00000335506.8:n.-562_-561insCC
ENST00000359373.9:c.509+4435_509+4436insCC	ENSP00000352332.5:n.509+4435_509+4436insCC
ENST00000393609.7:c.509+4435_509+4436insCC	ENSP00000377233.3:n.509+4435_509+4436insCC
NM_001040118.2:c.509+4435_509+4436insCC	NP_001035207.1:n.509+4435_509+4436insCC
NM_001135190.1:c.-562_-561insCC	NP_001128662.1:n.-562_-561insCC
NM_015242.4:c.-562_-561insCC	NP_056057.2:n.-562_-561insCC
NM_001369489.1:c.-562_-561insCC	NP_001356418.1:n.-562_-561insCC
NR_161388.1:n.156_157insCC
NM_001040118.3:c.509+4435_509+4436insCC MANE Select	NP_001035207.1:n.509+4435_509+4436insCC
NM_001135190.2:c.-562_-561insCC	NP_001128662.1:n.-562_-561insCC
NM_015242.5:c.-562_-561insCC	NP_056057.2:n.-562_-561insCC