Canonical Allele Identifier: CA6174133
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs759692897

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.851A>T MANE Select ENSP00000377233.3:p.Asp284Val
ENST00000334211.12:c.116A>T ENSP00000335506.8:p.Asp39Val
ENST00000359373.9:c.851A>T ENSP00000352332.5:p.Asp284Val
ENST00000393605.7:c.131A>T ENSP00000377230.3:p.Asp44Val
ENST00000393609.7:c.851A>T ENSP00000377233.3:p.Asp284Val
ENST00000426523.5:c.116A>T ENSP00000392264.1:p.Asp39Val
ENST00000429686.5:c.116A>T ENSP00000403127.1:p.Asp39Val
ENST00000465814.5:n.1188A>T
NM_001040118.2:c.851A>T NP_001035207.1:p.Asp284Val
NM_001135190.1:c.116A>T NP_001128662.1:p.Asp39Val
NM_015242.4:c.116A>T NP_056057.2:p.Asp39Val
NM_001369489.1:c.116A>T NP_001356418.1:p.Asp39Val
NR_161388.1:n.833A>T
NM_001040118.3:c.851A>T MANE Select NP_001035207.1:p.Asp284Val
NM_001135190.2:c.116A>T NP_001128662.1:p.Asp39Val
NM_015242.5:c.116A>T NP_056057.2:p.Asp39Val