Canonical Allele Identifier: CA2376021

Gene: ATRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48454401C>T , CM000665.2:g.48454401C>T	GRCh38
NC_000003.11:g.48495801C>T , CM000665.1:g.48495801C>T	GRCh37
NC_000003.10:g.48470805C>T	NCBI36
NG_041782.1:g.12692C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.654C>T MANE Select	ENSP00000323099.3:p.Pro218=
ENST00000634384.2:c.92C>T
ENST00000639561.1:c.*317C>T	ENSP00000491983.1:n.*317C>T
ENST00000320211.8:c.654C>T	ENSP00000323099.3:p.Pro218=
ENST00000346691.9:c.654C>T	ENSP00000302338.5:p.Pro218=
ENST00000357105.10:c.273C>T	ENSP00000349620.6:p.Pro91=
ENST00000412052.4:c.375C>T	ENSP00000400930.1:p.Pro125=
ENST00000634384.1:c.*317C>T	ENSP00000489041.1:n.*317C>T
ENST00000635082.1:c.375C>T	ENSP00000489136.1:p.Pro125=
ENST00000635084.1:n.44C>T
ENST00000635099.1:c.375C>T	ENSP00000489608.1:p.Pro125=
ENST00000635464.1:c.654C>T	ENSP00000489199.1:p.Pro218=
NM_001271022.1:c.273C>T	NP_001257951.1:p.Pro91=
NM_001271023.1:c.375C>T	NP_001257952.1:p.Pro125=
NM_032166.3:c.654C>T	NP_115542.2:p.Pro218=
NM_130384.2:c.654C>T	NP_569055.1:p.Pro218=
NR_153405.1:n.721C>T
NM_130384.3:c.654C>T MANE Select	NP_569055.1:p.Pro218=
NM_001271023.2:c.375C>T	NP_001257952.1:p.Pro125=
NM_032166.4:c.654C>T	NP_115542.2:p.Pro218=
NM_001271022.2:c.273C>T	NP_001257951.1:p.Pro91=