Canonical Allele Identifier: CA600098593

Gene: ARAP1

Linked Data

• dbSNP Id: rs1299850448
• gnomAD v2: 11-72433290-G-GTC
• gnomAD v3: 11-72722245-G-GTC
• gnomAD v4: 11-72722245-G-GTC
• MyVariant Identifiers: chr11:g.72433290_72433291insTC (hg19) ; chr11:g.72722245_72722246insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722246_72722247insCT , CM000673.2:g.72722246_72722247insCT	GRCh38
NC_000011.9:g.72433291_72433292insCT , CM000673.1:g.72433291_72433292insCT	GRCh37
NC_000011.8:g.72110939_72110940insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4374_509+4375insGA MANE Select	ENSP00000377233.3:n.509+4374_509+4375insGA
ENST00000334211.12:c.-623_-622insGA	ENSP00000335506.8:n.-623_-622insGA
ENST00000359373.9:c.509+4374_509+4375insGA	ENSP00000352332.5:n.509+4374_509+4375insGA
ENST00000393609.7:c.509+4374_509+4375insGA	ENSP00000377233.3:n.509+4374_509+4375insGA
NM_001040118.2:c.509+4374_509+4375insGA	NP_001035207.1:n.509+4374_509+4375insGA
NM_001135190.1:c.-623_-622insGA	NP_001128662.1:n.-623_-622insGA
NM_015242.4:c.-623_-622insGA	NP_056057.2:n.-623_-622insGA
NM_001369489.1:c.-623_-622insGA	NP_001356418.1:n.-623_-622insGA
NR_161388.1:n.95_96insGA
NM_001040118.3:c.509+4374_509+4375insGA MANE Select	NP_001035207.1:n.509+4374_509+4375insGA
NM_001135190.2:c.-623_-622insGA	NP_001128662.1:n.-623_-622insGA
NM_015242.5:c.-623_-622insGA	NP_056057.2:n.-623_-622insGA