Canonical Allele Identifier: CA2792663732

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712894A>G , CM000673.2:g.72712894A>G	GRCh38
NC_000011.9:g.72423939A>G , CM000673.1:g.72423939A>G	GRCh37
NC_000011.8:g.72101587A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.747+282T>C MANE Select	ENSP00000377233.3:n.747+282T>C
ENST00000334211.12:c.12+282T>C	ENSP00000335506.8:n.12+282T>C
ENST00000359373.9:c.747+282T>C	ENSP00000352332.5:n.747+282T>C
ENST00000393605.7:c.-299T>C	ENSP00000377230.3:n.-299T>C
ENST00000393609.7:c.747+282T>C	ENSP00000377233.3:n.747+282T>C
ENST00000426523.5:c.12+282T>C	ENSP00000392264.1:n.12+282T>C
ENST00000429686.5:c.12+282T>C	ENSP00000403127.1:n.12+282T>C
ENST00000465814.5:n.759T>C
NM_001040118.2:c.747+282T>C	NP_001035207.1:n.747+282T>C
NM_001135190.1:c.12+282T>C	NP_001128662.1:n.12+282T>C
NM_015242.4:c.12+282T>C	NP_056057.2:n.12+282T>C
NM_001369489.1:c.12+282T>C	NP_001356418.1:n.12+282T>C
NR_161388.1:n.729+282T>C
NM_001040118.3:c.747+282T>C MANE Select	NP_001035207.1:n.747+282T>C
NM_001135190.2:c.12+282T>C	NP_001128662.1:n.12+282T>C
NM_015242.5:c.12+282T>C	NP_056057.2:n.12+282T>C