Canonical Allele Identifier: CA2614978586

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722182-G-GGAGAGGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722187_72722188insGGAGAGAG , CM000673.2:g.72722187_72722188insGGAGAGAG	GRCh38
NC_000011.9:g.72433232_72433233insGGAGAGAG , CM000673.1:g.72433232_72433233insGGAGAGAG	GRCh37
NC_000011.8:g.72110880_72110881insGGAGAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4437_509+4438insTCCCTCTC MANE Select	ENSP00000377233.3:n.509+4437_509+4438insTCCCTCTC
ENST00000334211.12:c.-560_-559insTCCCTCTC	ENSP00000335506.8:n.-560_-559insTCCCTCTC
ENST00000359373.9:c.509+4437_509+4438insTCCCTCTC	ENSP00000352332.5:n.509+4437_509+4438insTCCCTCTC
ENST00000393609.7:c.509+4437_509+4438insTCCCTCTC	ENSP00000377233.3:n.509+4437_509+4438insTCCCTCTC
NM_001040118.2:c.509+4437_509+4438insTCCCTCTC	NP_001035207.1:n.509+4437_509+4438insTCCCTCTC
NM_001135190.1:c.-560_-559insTCCCTCTC	NP_001128662.1:n.-560_-559insTCCCTCTC
NM_015242.4:c.-560_-559insTCCCTCTC	NP_056057.2:n.-560_-559insTCCCTCTC
NM_001369489.1:c.-560_-559insTCCCTCTC	NP_001356418.1:n.-560_-559insTCCCTCTC
NR_161388.1:n.158_159insTCCCTCTC
NM_001040118.3:c.509+4437_509+4438insTCCCTCTC MANE Select	NP_001035207.1:n.509+4437_509+4438insTCCCTCTC
NM_001135190.2:c.-560_-559insTCCCTCTC	NP_001128662.1:n.-560_-559insTCCCTCTC
NM_015242.5:c.-560_-559insTCCCTCTC	NP_056057.2:n.-560_-559insTCCCTCTC