Canonical Allele Identifier: CA2639153817

Gene: BRIP1

Linked Data

• gnomAD v4: 17-61683571-C-CTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683571_61683572insTAT , CM000679.2:g.61683571_61683572insTAT	GRCh38
NC_000017.10:g.59760932_59760933insTAT , CM000679.1:g.59760932_59760933insTAT	GRCh37
NC_000017.9:g.57115714_57115715insTAT	NCBI36
NG_007409.2:g.184988_184989insATA , LRG_300:g.184988_184989insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2214_2215insATA
ENST00000682453.1:c.3474_3475insATA	ENSP00000506943.1:p.Leu1158_Ala1159insIle
ENST00000682477.1:c.*2900_*2901insATA	ENSP00000507075.1:n.*2900_*2901insATA
ENST00000682589.1:n.9351_9352insATA
ENST00000682755.1:c.3252_3253insATA	ENSP00000507660.1:p.Leu1084_Ala1085insIle
ENST00000682989.1:c.*565_*566insATA	ENSP00000507786.1:n.*565_*566insATA
ENST00000683039.1:c.3474_3475insATA	ENSP00000508303.1:p.Leu1158_Ala1159insIle
ENST00000683235.1:c.*889_*890insATA	ENSP00000507646.1:n.*889_*890insATA
ENST00000683535.1:n.1604_1605insATA
ENST00000684584.1:c.2637_2638insATA	ENSP00000508044.1:p.Leu879_Ala880insIle
ENST00000684626.1:n.1720_1721insATA
ENST00000684769.1:c.1664_1665insATA	ENSP00000507691.1:n.1664_1665insATA
ENST00000259008.7:c.3474_3475insATA MANE Select	ENSP00000259008.2:p.Leu1158_Ala1159insIle
ENST00000259008.6:c.3474_3475insATA	ENSP00000259008.2:p.Leu1158_Ala1159insIle
NM_032043.2:c.3474_3475insATA , LRG_300t1:c.3474_3475insATA	NP_114432.2:p.Leu1158_Ala1159insIle
XM_011525332.1:c.3534_3535insATA	XP_011523634.1:p.Leu1178_Ala1179insIle
XM_011525333.1:c.3534_3535insATA	XP_011523635.1:p.Leu1178_Ala1179insIle
XM_011525334.1:c.3534_3535insATA	XP_011523636.1:p.Leu1178_Ala1179insIle
XM_011525335.1:c.3474_3475insATA	XP_011523637.1:p.Leu1158_Ala1159insIle
XM_011525336.1:c.3414_3415insATA	XP_011523638.1:p.Leu1138_Ala1139insIle
XM_011525337.1:c.3333_3334insATA	XP_011523639.1:p.Leu1111_Ala1112insIle
XM_011525338.1:c.3051_3052insATA	XP_011523640.1:p.Leu1017_Ala1018insIle
XM_011525332.3:c.3534_3535insATA	XP_011523634.1:p.Leu1178_Ala1179insIle
XM_011525333.3:c.3534_3535insATA	XP_011523635.1:p.Leu1178_Ala1179insIle
XM_011525334.2:c.3534_3535insATA	XP_011523636.1:p.Leu1178_Ala1179insIle
XM_011525335.3:c.3474_3475insATA	XP_011523637.1:p.Leu1158_Ala1159insIle
XM_011525336.2:c.3414_3415insATA	XP_011523638.1:p.Leu1138_Ala1139insIle
XM_011525337.2:c.3333_3334insATA	XP_011523639.1:p.Leu1111_Ala1112insIle
XM_011525338.2:c.3051_3052insATA	XP_011523640.1:p.Leu1017_Ala1018insIle
XM_017025200.1:c.2991_2992insATA	XP_016880689.1:p.Leu997_Ala998insIle
XM_017025201.1:c.2991_2992insATA	XP_016880690.1:p.Leu997_Ala998insIle
XM_017025202.1:c.1620_1621insATA	XP_016880691.1:p.Leu540_Ala541insIle
XM_017025203.1:c.1620_1621insATA	XP_016880692.1:p.Leu540_Ala541insIle
NM_032043.3:c.3474_3475insATA MANE Select	NP_114432.2:p.Leu1158_Ala1159insIle