Canonical Allele Identifier: CA542785131

Gene: ATRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48449791del , CM000665.2:g.48449791del	GRCh38
NC_000003.11:g.48491197del , CM000665.1:g.48491197del	GRCh37
NC_000003.10:g.48466201del	NCBI36
NG_041782.1:g.8082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.248-246del MANE Select	ENSP00000323099.3:n.248-246del
ENST00000639561.1:c.-32-246del	ENSP00000491983.1:n.-32-246del
ENST00000320211.8:c.248-246del	ENSP00000323099.3:n.248-246del
ENST00000346691.9:c.248-246del	ENSP00000302338.5:n.248-246del
ENST00000357105.10:c.-217-246del	ENSP00000349620.6:n.-217-246del
ENST00000412052.4:c.-32-246del	ENSP00000400930.1:n.-32-246del
ENST00000634384.1:c.-32-246del	ENSP00000489041.1:n.-32-246del
ENST00000635082.1:c.-32-246del	ENSP00000489136.1:n.-32-246del
ENST00000635099.1:c.-32-246del	ENSP00000489608.1:n.-32-246del
ENST00000635464.1:c.248-246del	ENSP00000489199.1:n.248-246del
NM_001271022.1:c.-217-246del	NP_001257951.1:n.-217-246del
NM_001271023.1:c.-32-246del	NP_001257952.1:n.-32-246del
NM_032166.3:c.248-246del	NP_115542.2:n.248-246del
NM_130384.2:c.248-246del	NP_569055.1:n.248-246del
NR_153405.1:n.315-246del
NM_130384.3:c.248-246del MANE Select	NP_569055.1:n.248-246del
NM_001271023.2:c.-32-246del	NP_001257952.1:n.-32-246del
NM_032166.4:c.248-246del	NP_115542.2:n.248-246del
NM_001271022.2:c.-217-246del	NP_001257951.1:n.-217-246del