Canonical Allele Identifier: CA400479415

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59793322C>A (hg19) ; chr17:g.61715961C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61715961C>A , CM000679.2:g.61715961C>A	GRCh38
NC_000017.10:g.59793322C>A , CM000679.1:g.59793322C>A	GRCh37
NC_000017.9:g.57148104C>A	NCBI36
NG_007409.2:g.152599G>T , LRG_300:g.152599G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2612G>T	ENSP00000507191.1:n.2612G>T
ENST00000682073.1:n.1222G>T
ENST00000682433.1:n.1561G>T
ENST00000682453.1:c.2482G>T	ENSP00000506943.1:p.Ala828Ser
ENST00000682477.1:c.*1908G>T	ENSP00000507075.1:n.*1908G>T
ENST00000682589.1:n.8359G>T
ENST00000682755.1:c.2260G>T	ENSP00000507660.1:p.Ala754Ser
ENST00000682989.1:c.2482G>T	ENSP00000507786.1:p.Ala828Ser
ENST00000683039.1:c.2482G>T	ENSP00000508303.1:p.Ala828Ser
ENST00000683235.1:c.2482G>T	ENSP00000507646.1:p.Ala828Ser
ENST00000683535.1:n.612G>T
ENST00000684471.1:n.895G>T
ENST00000684584.1:c.1975G>T	ENSP00000508044.1:p.Ala659Ser
ENST00000684626.1:n.811G>T
ENST00000684769.1:c.547G>T	ENSP00000507691.1:p.Ala183Ser
ENST00000259008.7:c.2482G>T MANE Select	ENSP00000259008.2:p.Ala828Ser
ENST00000259008.6:c.2482G>T	ENSP00000259008.2:p.Ala828Ser
ENST00000577598.5:c.2482G>T	ENSP00000464654.1:p.Ala828Ser
NM_032043.2:c.2482G>T , LRG_300t1:c.2482G>T	NP_114432.2:p.Ala828Ser
XM_011525332.1:c.2542G>T	XP_011523634.1:p.Ala848Ser
XM_011525333.1:c.2542G>T	XP_011523635.1:p.Ala848Ser
XM_011525334.1:c.2542G>T	XP_011523636.1:p.Ala848Ser
XM_011525335.1:c.2482G>T	XP_011523637.1:p.Ala828Ser
XM_011525336.1:c.2422G>T	XP_011523638.1:p.Ala808Ser
XM_011525337.1:c.2341G>T	XP_011523639.1:p.Ala781Ser
XM_011525338.1:c.2059G>T	XP_011523640.1:p.Ala687Ser
XM_011525340.1:c.2542G>T	XP_011523642.1:p.Ala848Ser
XM_011525332.3:c.2542G>T	XP_011523634.1:p.Ala848Ser
XM_011525333.3:c.2542G>T	XP_011523635.1:p.Ala848Ser
XM_011525334.2:c.2542G>T	XP_011523636.1:p.Ala848Ser
XM_011525335.3:c.2482G>T	XP_011523637.1:p.Ala828Ser
XM_011525336.2:c.2422G>T	XP_011523638.1:p.Ala808Ser
XM_011525337.2:c.2341G>T	XP_011523639.1:p.Ala781Ser
XM_011525338.2:c.2059G>T	XP_011523640.1:p.Ala687Ser
XM_011525340.3:c.2542G>T	XP_011523642.1:p.Ala848Ser
XM_017025200.1:c.1999G>T	XP_016880689.1:p.Ala667Ser
XM_017025201.1:c.1999G>T	XP_016880690.1:p.Ala667Ser
XM_017025202.1:c.628G>T	XP_016880691.1:p.Ala210Ser
XM_017025203.1:c.628G>T	XP_016880692.1:p.Ala210Ser
NM_032043.3:c.2482G>T MANE Select	NP_114432.2:p.Ala828Ser