Canonical Allele Identifier: CA2269130855

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683568T= , CM000679.2:g.61683568T=	GRCh38
NC_000017.10:g.59760929T= , CM000679.1:g.59760929T=	GRCh37
NC_000017.9:g.57115711T=	NCBI36
NG_007409.2:g.184992A= , LRG_300:g.184992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2218A=
ENST00000682453.1:c.3478A=	ENSP00000506943.1:p.Asn1160=
ENST00000682477.1:c.*2904A=	ENSP00000507075.1:n.*2904A=
ENST00000682589.1:n.9355A=
ENST00000682755.1:c.3256A=	ENSP00000507660.1:p.Asn1086=
ENST00000682989.1:c.*569A=	ENSP00000507786.1:n.*569A=
ENST00000683039.1:c.3478A=	ENSP00000508303.1:p.Asn1160=
ENST00000683235.1:c.*893A=	ENSP00000507646.1:n.*893A=
ENST00000683535.1:n.1608A=
ENST00000684584.1:c.2641A=	ENSP00000508044.1:p.Asn881=
ENST00000684626.1:n.1724A=
ENST00000684769.1:c.1668A=	ENSP00000507691.1:n.1668A=
ENST00000259008.7:c.3478A= MANE Select	ENSP00000259008.2:p.Asn1160=
ENST00000259008.6:c.3478A=	ENSP00000259008.2:p.Asn1160=
NM_032043.2:c.3478A= , LRG_300t1:c.3478A=	NP_114432.2:p.Asn1160=
XM_011525332.1:c.3538A=	XP_011523634.1:p.Asn1180=
XM_011525333.1:c.3538A=	XP_011523635.1:p.Asn1180=
XM_011525334.1:c.3538A=	XP_011523636.1:p.Asn1180=
XM_011525335.1:c.3478A=	XP_011523637.1:p.Asn1160=
XM_011525336.1:c.3418A=	XP_011523638.1:p.Asn1140=
XM_011525337.1:c.3337A=	XP_011523639.1:p.Asn1113=
XM_011525338.1:c.3055A=	XP_011523640.1:p.Asn1019=
XM_011525332.3:c.3538A=	XP_011523634.1:p.Asn1180=
XM_011525333.3:c.3538A=	XP_011523635.1:p.Asn1180=
XM_011525334.2:c.3538A=	XP_011523636.1:p.Asn1180=
XM_011525335.3:c.3478A=	XP_011523637.1:p.Asn1160=
XM_011525336.2:c.3418A=	XP_011523638.1:p.Asn1140=
XM_011525337.2:c.3337A=	XP_011523639.1:p.Asn1113=
XM_011525338.2:c.3055A=	XP_011523640.1:p.Asn1019=
XM_017025200.1:c.2995A=	XP_016880689.1:p.Asn999=
XM_017025201.1:c.2995A=	XP_016880690.1:p.Asn999=
XM_017025202.1:c.1624A=	XP_016880691.1:p.Asn542=
XM_017025203.1:c.1624A=	XP_016880692.1:p.Asn542=
NM_032043.3:c.3478A= MANE Select	NP_114432.2:p.Asn1160=