Canonical Allele Identifier: CA2810059914

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683579_61683590del , CM000679.2:g.61683579_61683590del	GRCh38
NC_000017.10:g.59760940_59760951del , CM000679.1:g.59760940_59760951del	GRCh37
NC_000017.9:g.57115722_57115733del	NCBI36
NG_007409.2:g.184971_184982del , LRG_300:g.184971_184982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2197_2208del
ENST00000682453.1:c.3457_3468del	ENSP00000506943.1:p.Asp1153_Asn1156del
ENST00000682477.1:c.*2883_*2894del	ENSP00000507075.1:n.*2883_*2894del
ENST00000682589.1:n.9334_9345del
ENST00000682755.1:c.3235_3246del	ENSP00000507660.1:p.Asp1079_Asn1082del
ENST00000682989.1:c.*548_*559del	ENSP00000507786.1:n.*548_*559del
ENST00000683039.1:c.3457_3468del	ENSP00000508303.1:p.Asp1153_Asn1156del
ENST00000683235.1:c.*872_*883del	ENSP00000507646.1:n.*872_*883del
ENST00000683535.1:n.1587_1598del
ENST00000684584.1:c.2620_2631del	ENSP00000508044.1:p.Asp874_Asn877del
ENST00000684626.1:n.1703_1714del
ENST00000684769.1:c.1647_1658del	ENSP00000507691.1:n.1647_1658del
ENST00000259008.7:c.3457_3468del MANE Select	ENSP00000259008.2:p.Asp1153_Asn1156del
ENST00000259008.6:c.3457_3468del	ENSP00000259008.2:p.Asp1153_Asn1156del
NM_032043.2:c.3457_3468del , LRG_300t1:c.3457_3468del	NP_114432.2:p.Asp1153_Asn1156del
XM_011525332.1:c.3517_3528del	XP_011523634.1:p.Asp1173_Asn1176del
XM_011525333.1:c.3517_3528del	XP_011523635.1:p.Asp1173_Asn1176del
XM_011525334.1:c.3517_3528del	XP_011523636.1:p.Asp1173_Asn1176del
XM_011525335.1:c.3457_3468del	XP_011523637.1:p.Asp1153_Asn1156del
XM_011525336.1:c.3397_3408del	XP_011523638.1:p.Asp1133_Asn1136del
XM_011525337.1:c.3316_3327del	XP_011523639.1:p.Asp1106_Asn1109del
XM_011525338.1:c.3034_3045del	XP_011523640.1:p.Asp1012_Asn1015del
XM_011525332.3:c.3517_3528del	XP_011523634.1:p.Asp1173_Asn1176del
XM_011525333.3:c.3517_3528del	XP_011523635.1:p.Asp1173_Asn1176del
XM_011525334.2:c.3517_3528del	XP_011523636.1:p.Asp1173_Asn1176del
XM_011525335.3:c.3457_3468del	XP_011523637.1:p.Asp1153_Asn1156del
XM_011525336.2:c.3397_3408del	XP_011523638.1:p.Asp1133_Asn1136del
XM_011525337.2:c.3316_3327del	XP_011523639.1:p.Asp1106_Asn1109del
XM_011525338.2:c.3034_3045del	XP_011523640.1:p.Asp1012_Asn1015del
XM_017025200.1:c.2974_2985del	XP_016880689.1:p.Asp992_Asn995del
XM_017025201.1:c.2974_2985del	XP_016880690.1:p.Asp992_Asn995del
XM_017025202.1:c.1603_1614del	XP_016880691.1:p.Asp535_Asn538del
XM_017025203.1:c.1603_1614del	XP_016880692.1:p.Asp535_Asn538del
NM_032043.3:c.3457_3468del MANE Select	NP_114432.2:p.Asp1153_Asn1156del