Canonical Allele Identifier: CA2614979744

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72712476-ATCCCCTTGGTCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712482_72712493del , CM000673.2:g.72712482_72712493del	GRCh38
NC_000011.9:g.72423527_72423538del , CM000673.1:g.72423527_72423538del	GRCh37
NC_000011.8:g.72101175_72101186del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.828_839del MANE Select	ENSP00000377233.3:p.Asp277_Asp280del
ENST00000334211.12:c.93_104del	ENSP00000335506.8:p.Asp32_Asp35del
ENST00000359373.9:c.828_839del	ENSP00000352332.5:p.Asp277_Asp280del
ENST00000393605.7:c.108_119del	ENSP00000377230.3:p.Asp37_Asp40del
ENST00000393609.7:c.828_839del	ENSP00000377233.3:p.Asp277_Asp280del
ENST00000426523.5:c.93_104del	ENSP00000392264.1:p.Asp32_Asp35del
ENST00000429686.5:c.93_104del	ENSP00000403127.1:p.Asp32_Asp35del
ENST00000465814.5:n.1165_1176del
NM_001040118.2:c.828_839del	NP_001035207.1:p.Asp277_Asp280del
NM_001135190.1:c.93_104del	NP_001128662.1:p.Asp32_Asp35del
NM_015242.4:c.93_104del	NP_056057.2:p.Asp32_Asp35del
NM_001369489.1:c.93_104del	NP_001356418.1:p.Asp32_Asp35del
NR_161388.1:n.810_821del
NM_001040118.3:c.828_839del MANE Select	NP_001035207.1:p.Asp277_Asp280del
NM_001135190.2:c.93_104del	NP_001128662.1:p.Asp32_Asp35del
NM_015242.5:c.93_104del	NP_056057.2:p.Asp32_Asp35del