Canonical Allele Identifier: CA2375985

Gene: ATRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48451803G>A , CM000665.2:g.48451803G>A	GRCh38
NC_000003.11:g.48493209G>A , CM000665.1:g.48493209G>A	GRCh37
NC_000003.10:g.48468213G>A	NCBI36
NG_041782.1:g.10094G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_130384.3:c.456G>A MANE Select	NP_569055.1:p.Thr152=
ENST00000320211.10:c.456G>A MANE Select	ENSP00000323099.3:p.Thr152=
NM_001271022.1:c.75G>A	NP_001257951.1:p.Thr25=
NM_001271022.2:c.75G>A	NP_001257951.1:p.Thr25=
NM_001271023.1:c.177G>A	NP_001257952.1:p.Thr59=
NM_001271023.2:c.177G>A	NP_001257952.1:p.Thr59=
NM_032166.3:c.456G>A	NP_115542.2:p.Thr152=
NM_032166.4:c.456G>A	NP_115542.2:p.Thr152=
NM_130384.2:c.456G>A	NP_569055.1:p.Thr152=
NR_153405.1:n.523G>A
ENST00000320211.8:c.456G>A	ENSP00000323099.3:p.Thr152=
ENST00000346691.9:c.456G>A	ENSP00000302338.5:p.Thr152=
ENST00000357105.10:c.75G>A	ENSP00000349620.6:p.Thr25=
ENST00000412052.4:c.177G>A	ENSP00000400930.1:p.Thr59=
ENST00000634384.1:c.*119G>A	ENSP00000489041.1:n.*119G>A
ENST00000635082.1:c.177G>A	ENSP00000489136.1:p.Thr59=
ENST00000635099.1:c.177G>A	ENSP00000489608.1:p.Thr59=
ENST00000635464.1:c.456G>A	ENSP00000489199.1:p.Thr152=
ENST00000639561.1:c.*119G>A	ENSP00000491983.1:n.*119G>A