Canonical Allele Identifier: CA1982112498

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712488G= , CM000673.2:g.72712488G=	GRCh38
NC_000011.9:g.72423533G= , CM000673.1:g.72423533G=	GRCh37
NC_000011.8:g.72101181G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.828C= MANE Select	ENSP00000377233.3:p.Asp276=
ENST00000334211.12:c.93C=	ENSP00000335506.8:p.Asp31=
ENST00000359373.9:c.828C=	ENSP00000352332.5:p.Asp276=
ENST00000393605.7:c.108C=	ENSP00000377230.3:p.Asp36=
ENST00000393609.7:c.828C=	ENSP00000377233.3:p.Asp276=
ENST00000426523.5:c.93C=	ENSP00000392264.1:p.Asp31=
ENST00000429686.5:c.93C=	ENSP00000403127.1:p.Asp31=
ENST00000465814.5:n.1165C=
NM_001040118.2:c.828C=	NP_001035207.1:p.Asp276=
NM_001135190.1:c.93C=	NP_001128662.1:p.Asp31=
NM_015242.4:c.93C=	NP_056057.2:p.Asp31=
NM_001369489.1:c.93C=	NP_001356418.1:p.Asp31=
NR_161388.1:n.810C=
NM_001040118.3:c.828C= MANE Select	NP_001035207.1:p.Asp276=
NM_001135190.2:c.93C=	NP_001128662.1:p.Asp31=
NM_015242.5:c.93C=	NP_056057.2:p.Asp31=