Canonical Allele Identifier: CA1982116825

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722082G= , CM000673.2:g.72722082G=	GRCh38
NC_000011.9:g.72433127G= , CM000673.1:g.72433127G=	GRCh37
NC_000011.8:g.72110775G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4538C= MANE Select	ENSP00000377233.3:n.509+4538C=
ENST00000334211.12:c.-459C=	ENSP00000335506.8:n.-459C=
ENST00000359373.9:c.509+4538C=	ENSP00000352332.5:n.509+4538C=
ENST00000393609.7:c.509+4538C=	ENSP00000377233.3:n.509+4538C=
ENST00000465814.5:n.7C=
NM_001040118.2:c.509+4538C=	NP_001035207.1:n.509+4538C=
NM_001135190.1:c.-459C=	NP_001128662.1:n.-459C=
NM_015242.4:c.-459C=	NP_056057.2:n.-459C=
NM_001369489.1:c.-459C=	NP_001356418.1:n.-459C=
NR_161388.1:n.259C=
NM_001040118.3:c.509+4538C= MANE Select	NP_001035207.1:n.509+4538C=
NM_001135190.2:c.-459C=	NP_001128662.1:n.-459C=
NM_015242.5:c.-459C=	NP_056057.2:n.-459C=