Canonical Allele Identifier: CA1982112489

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712465T= , CM000673.2:g.72712465T=	GRCh38
NC_000011.9:g.72423510T= , CM000673.1:g.72423510T=	GRCh37
NC_000011.8:g.72101158T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.851A= MANE Select	ENSP00000377233.3:p.Asp284=
ENST00000334211.12:c.116A=	ENSP00000335506.8:p.Asp39=
ENST00000359373.9:c.851A=	ENSP00000352332.5:p.Asp284=
ENST00000393605.7:c.131A=	ENSP00000377230.3:p.Asp44=
ENST00000393609.7:c.851A=	ENSP00000377233.3:p.Asp284=
ENST00000426523.5:c.116A=	ENSP00000392264.1:p.Asp39=
ENST00000429686.5:c.116A=	ENSP00000403127.1:p.Asp39=
ENST00000465814.5:n.1188A=
NM_001040118.2:c.851A=	NP_001035207.1:p.Asp284=
NM_001135190.1:c.116A=	NP_001128662.1:p.Asp39=
NM_015242.4:c.116A=	NP_056057.2:p.Asp39=
NM_001369489.1:c.116A=	NP_001356418.1:p.Asp39=
NR_161388.1:n.833A=
NM_001040118.3:c.851A= MANE Select	NP_001035207.1:p.Asp284=
NM_001135190.2:c.116A=	NP_001128662.1:p.Asp39=
NM_015242.5:c.116A=	NP_056057.2:p.Asp39=