Canonical Allele Identifier: CA2885369

Gene: ARAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.36228714T>C , CM000666.2:g.36228714T>C	GRCh38
NC_000004.11:g.36230336T>C , CM000666.1:g.36230336T>C	GRCh37
NC_000004.10:g.35906731T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015230.4:c.773A>G MANE Select	NP_056045.2:p.Tyr258Cys
ENST00000303965.9:c.773A>G MANE Select	ENSP00000302895.4:p.Tyr258Cys
NM_015230.3:c.773A>G	NP_056045.2:p.Tyr258Cys
NR_146893.1:n.1263A>G
NR_146893.2:n.1263A>G
NR_146894.1:n.1261A>G
NR_146894.2:n.1268A>G
ENST00000303965.8:c.773A>G	ENSP00000302895.4:p.Tyr258Cys
ENST00000508066.1:n.1104A>G
XM_005262642.2:c.773A>G	XP_005262699.1:p.Tyr258Cys
XM_017007699.1:c.773A>G	XP_016863188.1:p.Tyr258Cys
XM_017007700.1:c.773A>G	XP_016863189.1:p.Tyr258Cys
XM_017007701.1:c.773A>G	XP_016863190.1:p.Tyr258Cys
XM_017007702.1:c.773A>G	XP_016863191.1:p.Tyr258Cys
XR_001741104.1:n.1541A>G
XR_001741105.1:n.1541A>G
XR_001741106.1:n.1541A>G
XR_001741107.1:n.1541A>G
XR_001741108.1:n.1541A>G
XR_001741109.1:n.1541A>G
XR_001741110.2:n.1728A>G
XR_001741111.2:n.1056A>G
XR_001741112.2:n.1010A>G
XR_001741113.1:n.1104A>G
XR_001741115.1:n.1541A>G
XR_001741116.1:n.1541A>G
XR_001741117.1:n.1541A>G
XR_001741118.1:n.1541A>G
XR_001741119.1:n.1541A>G
XR_001741120.1:n.1541A>G
XR_001741121.1:n.1541A>G
XR_001741122.1:n.1541A>G