Canonical Allele Identifier: CA1982112472

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712439_72712440delinsTG , CM000673.2:g.72712439_72712440delinsTG	GRCh38
NC_000011.9:g.72423484_72423485delinsTG , CM000673.1:g.72423484_72423485delinsTG	GRCh37
NC_000011.8:g.72101132_72101133delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.876_877delinsCA MANE Select	ENSP00000377233.3:p.Pro292=
ENST00000334211.12:c.141_142delinsCA	ENSP00000335506.8:p.Pro47=
ENST00000359373.9:c.876_877delinsCA	ENSP00000352332.5:p.Pro292=
ENST00000393605.7:c.156_157delinsCA	ENSP00000377230.3:p.Pro52=
ENST00000393609.7:c.876_877delinsCA	ENSP00000377233.3:p.Pro292=
ENST00000426523.5:c.141_142delinsCA	ENSP00000392264.1:p.Pro47=
ENST00000429686.5:c.141_142delinsCA	ENSP00000403127.1:p.Pro47=
ENST00000465814.5:n.1213_1214delinsCA
NM_001040118.2:c.876_877delinsCA	NP_001035207.1:p.Pro292=
NM_001135190.1:c.141_142delinsCA	NP_001128662.1:p.Pro47=
NM_015242.4:c.141_142delinsCA	NP_056057.2:p.Pro47=
NM_001369489.1:c.141_142delinsCA	NP_001356418.1:p.Pro47=
NR_161388.1:n.858_859delinsCA
NM_001040118.3:c.876_877delinsCA MANE Select	NP_001035207.1:p.Pro292=
NM_001135190.2:c.141_142delinsCA	NP_001128662.1:p.Pro47=
NM_015242.5:c.141_142delinsCA	NP_056057.2:p.Pro47=