Canonical Allele Identifier: CA2614979777

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72712533-CACG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712534_72712536del , CM000673.2:g.72712534_72712536del	GRCh38
NC_000011.9:g.72423579_72423581del , CM000673.1:g.72423579_72423581del	GRCh37
NC_000011.8:g.72101227_72101229del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.780_782del MANE Select	ENSP00000377233.3:p.Val261del
ENST00000334211.12:c.45_47del	ENSP00000335506.8:p.Val16del
ENST00000359373.9:c.780_782del	ENSP00000352332.5:p.Val261del
ENST00000393605.7:c.60_62del	ENSP00000377230.3:p.Val21del
ENST00000393609.7:c.780_782del	ENSP00000377233.3:p.Val261del
ENST00000426523.5:c.45_47del	ENSP00000392264.1:p.Val16del
ENST00000429686.5:c.45_47del	ENSP00000403127.1:p.Val16del
ENST00000465814.5:n.1117_1119del
NM_001040118.2:c.780_782del	NP_001035207.1:p.Val261del
NM_001135190.1:c.45_47del	NP_001128662.1:p.Val16del
NM_015242.4:c.45_47del	NP_056057.2:p.Val16del
NM_001369489.1:c.45_47del	NP_001356418.1:p.Val16del
NR_161388.1:n.762_764del
NM_001040118.3:c.780_782del MANE Select	NP_001035207.1:p.Val261del
NM_001135190.2:c.45_47del	NP_001128662.1:p.Val16del
NM_015242.5:c.45_47del	NP_056057.2:p.Val16del