Canonical Allele Identifier: CA15330870

Gene: ARAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.36077972T>C , CM000666.2:g.36077972T>C	GRCh38
NC_000004.11:g.36079594T>C , CM000666.1:g.36079594T>C	GRCh37
NC_000004.10:g.35755989T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303965.9:c.4608+2244A>G MANE Select	ENSP00000302895.4:n.4608+2244A>G
ENST00000303965.8:c.4608+2244A>G	ENSP00000302895.4:n.4608+2244A>G
ENST00000618163.1:c.2385+2244A>G	ENSP00000481036.1:n.2385+2244A>G
NM_015230.3:c.4608+2244A>G	NP_056045.2:n.4608+2244A>G
NR_146893.1:n.5098+2244A>G
NR_146894.1:n.5062+2244A>G
XM_017007699.1:c.4608+2244A>G	XP_016863188.1:n.4608+2244A>G
XM_017007700.1:c.4539+2244A>G	XP_016863189.1:n.4539+2244A>G
XM_017007701.1:c.4608+2244A>G	XP_016863190.1:n.4608+2244A>G
XM_017007702.1:c.4539+2244A>G	XP_016863191.1:n.4539+2244A>G
XR_001741104.1:n.5376+2244A>G
XR_001741105.1:n.5376+2244A>G
XR_001741106.1:n.5376+2244A>G
XR_001741107.1:n.5376+2244A>G
XR_001741108.1:n.5376+2244A>G
XR_001741109.1:n.5376+2244A>G
XR_001741110.2:n.5563+2244A>G
XR_001741111.2:n.4891+2244A>G
XR_001741112.2:n.4845+2244A>G
XR_001741113.1:n.4939+2244A>G
XR_001741115.1:n.5343+2244A>G
XR_001741116.1:n.5307+2244A>G
XR_001741117.1:n.5376+2244A>G
XR_001741118.1:n.5376+2244A>G
XR_001741119.1:n.5376+2244A>G
XR_001741120.1:n.5376+2244A>G
XR_001741121.1:n.5376+2244A>G
XR_001741122.1:n.5307+2244A>G
XR_001741123.1:n.2854+2244A>G
NM_015230.4:c.4608+2244A>G MANE Select	NP_056045.2:n.4608+2244A>G
NR_146893.2:n.5098+2244A>G
NR_146894.2:n.5069+2244A>G