Canonical Allele Identifier: CA1982116873

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722169G= , CM000673.2:g.72722169G=	GRCh38
NC_000011.9:g.72433214G= , CM000673.1:g.72433214G=	GRCh37
NC_000011.8:g.72110862G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4451C= MANE Select	ENSP00000377233.3:n.509+4451C=
ENST00000334211.12:c.-546C=	ENSP00000335506.8:n.-546C=
ENST00000359373.9:c.509+4451C=	ENSP00000352332.5:n.509+4451C=
ENST00000393609.7:c.509+4451C=	ENSP00000377233.3:n.509+4451C=
NM_001040118.2:c.509+4451C=	NP_001035207.1:n.509+4451C=
NM_001135190.1:c.-546C=	NP_001128662.1:n.-546C=
NM_015242.4:c.-546C=	NP_056057.2:n.-546C=
NM_001369489.1:c.-546C=	NP_001356418.1:n.-546C=
NR_161388.1:n.172C=
NM_001040118.3:c.509+4451C= MANE Select	NP_001035207.1:n.509+4451C=
NM_001135190.2:c.-546C=	NP_001128662.1:n.-546C=
NM_015242.5:c.-546C=	NP_056057.2:n.-546C=