Canonical Allele Identifier: CA600098590

Gene: ARAP1

Linked Data

• dbSNP Id: rs1565226347
• gnomAD v2: 11-72433241-A-AGT
• gnomAD v3: 11-72722196-A-AGT
• gnomAD v4: 11-72722196-A-AGT
• MyVariant Identifiers: chr11:g.72433241_72433242insGT (hg19) ; chr11:g.72722196_72722197insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722204_72722205dup , CM000673.2:g.72722204_72722205dup	GRCh38
NC_000011.9:g.72433249_72433250dup , CM000673.1:g.72433249_72433250dup	GRCh37
NC_000011.8:g.72110897_72110898dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4422_509+4423dup MANE Select	ENSP00000377233.3:n.509+4422_509+4423dup
ENST00000334211.12:c.-575_-574dup	ENSP00000335506.8:n.-575_-574dup
ENST00000359373.9:c.509+4422_509+4423dup	ENSP00000352332.5:n.509+4422_509+4423dup
ENST00000393609.7:c.509+4422_509+4423dup	ENSP00000377233.3:n.509+4422_509+4423dup
NM_001040118.2:c.509+4422_509+4423dup	NP_001035207.1:n.509+4422_509+4423dup
NM_001135190.1:c.-575_-574dup	NP_001128662.1:n.-575_-574dup
NM_015242.4:c.-575_-574dup	NP_056057.2:n.-575_-574dup
NM_001369489.1:c.-575_-574dup	NP_001356418.1:n.-575_-574dup
NR_161388.1:n.143_144dup
NM_001040118.3:c.509+4422_509+4423dup MANE Select	NP_001035207.1:n.509+4422_509+4423dup
NM_001135190.2:c.-575_-574dup	NP_001128662.1:n.-575_-574dup
NM_015242.5:c.-575_-574dup	NP_056057.2:n.-575_-574dup