Canonical Allele Identifier: CA2614978653

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722194-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722195_72722196insTG , CM000673.2:g.72722195_72722196insTG	GRCh38
NC_000011.9:g.72433240_72433241insTG , CM000673.1:g.72433240_72433241insTG	GRCh37
NC_000011.8:g.72110888_72110889insTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4425_509+4426insAC MANE Select	ENSP00000377233.3:n.509+4425_509+4426insAC
ENST00000334211.12:c.-572_-571insAC	ENSP00000335506.8:n.-572_-571insAC
ENST00000359373.9:c.509+4425_509+4426insAC	ENSP00000352332.5:n.509+4425_509+4426insAC
ENST00000393609.7:c.509+4425_509+4426insAC	ENSP00000377233.3:n.509+4425_509+4426insAC
NM_001040118.2:c.509+4425_509+4426insAC	NP_001035207.1:n.509+4425_509+4426insAC
NM_001135190.1:c.-572_-571insAC	NP_001128662.1:n.-572_-571insAC
NM_015242.4:c.-572_-571insAC	NP_056057.2:n.-572_-571insAC
NM_001369489.1:c.-572_-571insAC	NP_001356418.1:n.-572_-571insAC
NR_161388.1:n.146_147insAC
NM_001040118.3:c.509+4425_509+4426insAC MANE Select	NP_001035207.1:n.509+4425_509+4426insAC
NM_001135190.2:c.-572_-571insAC	NP_001128662.1:n.-572_-571insAC
NM_015242.5:c.-572_-571insAC	NP_056057.2:n.-572_-571insAC