Canonical Allele Identifier: CA1982116879

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722173_72722177delinsAAGAC , CM000673.2:g.72722173_72722177delinsAAGAC	GRCh38
NC_000011.9:g.72433218_72433222delinsAAGAC , CM000673.1:g.72433218_72433222delinsAAGAC	GRCh37
NC_000011.8:g.72110866_72110870delinsAAGAC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4443_509+4447delinsGTCTT MANE Select	ENSP00000377233.3:n.509+4443_509+4447deli...
ENST00000334211.12:c.-554_-550delinsGTCTT	ENSP00000335506.8:n.-554_-550delinsGTCTT
ENST00000359373.9:c.509+4443_509+4447delinsGTCTT	ENSP00000352332.5:n.509+4443_509+4447deli...
ENST00000393609.7:c.509+4443_509+4447delinsGTCTT	ENSP00000377233.3:n.509+4443_509+4447deli...
NM_001040118.2:c.509+4443_509+4447delinsGTCTT	NP_001035207.1:n.509+4443_509+4447delinsG...
NM_001135190.1:c.-554_-550delinsGTCTT	NP_001128662.1:n.-554_-550delinsGTCTT
NM_015242.4:c.-554_-550delinsGTCTT	NP_056057.2:n.-554_-550delinsGTCTT
NM_001369489.1:c.-554_-550delinsGTCTT	NP_001356418.1:n.-554_-550delinsGTCTT
NR_161388.1:n.164_168delinsGTCTT
NM_001040118.3:c.509+4443_509+4447delinsGTCTT MANE Select	NP_001035207.1:n.509+4443_509+4447delinsG...
NM_001135190.2:c.-554_-550delinsGTCTT	NP_001128662.1:n.-554_-550delinsGTCTT
NM_015242.5:c.-554_-550delinsGTCTT	NP_056057.2:n.-554_-550delinsGTCTT