Canonical Allele Identifier: CA2614979688

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72712458-GTGGTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712460_72712465del , CM000673.2:g.72712460_72712465del	GRCh38
NC_000011.9:g.72423505_72423510del , CM000673.1:g.72423505_72423510del	GRCh37
NC_000011.8:g.72101153_72101158del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.852_857del MANE Select	ENSP00000377233.3:p.Asp285_His286del
ENST00000334211.12:c.117_122del	ENSP00000335506.8:p.Asp40_His41del
ENST00000359373.9:c.852_857del	ENSP00000352332.5:p.Asp285_His286del
ENST00000393605.7:c.132_137del	ENSP00000377230.3:p.Asp45_His46del
ENST00000393609.7:c.852_857del	ENSP00000377233.3:p.Asp285_His286del
ENST00000426523.5:c.117_122del	ENSP00000392264.1:p.Asp40_His41del
ENST00000429686.5:c.117_122del	ENSP00000403127.1:p.Asp40_His41del
ENST00000465814.5:n.1189_1194del
NM_001040118.2:c.852_857del	NP_001035207.1:p.Asp285_His286del
NM_001135190.1:c.117_122del	NP_001128662.1:p.Asp40_His41del
NM_015242.4:c.117_122del	NP_056057.2:p.Asp40_His41del
NM_001369489.1:c.117_122del	NP_001356418.1:p.Asp40_His41del
NR_161388.1:n.834_839del
NM_001040118.3:c.852_857del MANE Select	NP_001035207.1:p.Asp285_His286del
NM_001135190.2:c.117_122del	NP_001128662.1:p.Asp40_His41del
NM_015242.5:c.117_122del	NP_056057.2:p.Asp40_His41del