Canonical Allele Identifier: CA1982116921

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722219C= , CM000673.2:g.72722219C=	GRCh38
NC_000011.9:g.72433264C= , CM000673.1:g.72433264C=	GRCh37
NC_000011.8:g.72110912C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4401G= MANE Select	ENSP00000377233.3:n.509+4401G=
ENST00000334211.12:c.-596G=	ENSP00000335506.8:n.-596G=
ENST00000359373.9:c.509+4401G=	ENSP00000352332.5:n.509+4401G=
ENST00000393609.7:c.509+4401G=	ENSP00000377233.3:n.509+4401G=
NM_001040118.2:c.509+4401G=	NP_001035207.1:n.509+4401G=
NM_001135190.1:c.-596G=	NP_001128662.1:n.-596G=
NM_015242.4:c.-596G=	NP_056057.2:n.-596G=
NM_001369489.1:c.-596G=	NP_001356418.1:n.-596G=
NR_161388.1:n.122G=
NM_001040118.3:c.509+4401G= MANE Select	NP_001035207.1:n.509+4401G=
NM_001135190.2:c.-596G=	NP_001128662.1:n.-596G=
NM_015242.5:c.-596G=	NP_056057.2:n.-596G=