Canonical Allele Identifier: CA400483651

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 649616
• ClinVar RCV Id: RCV000804596
• dbSNP Id: rs587782247
• MyVariant Identifiers: chr17:g.59876575C>G (hg19) ; chr17:g.61799214C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61799214C>G , CM000679.2:g.61799214C>G	GRCh38
NC_000017.10:g.59876575C>G , CM000679.1:g.59876575C>G	GRCh37
NC_000017.9:g.57231357C>G	NCBI36
NG_007409.2:g.69346G>C , LRG_300:g.69346G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.719G>C	ENSP00000463827.2:p.Ser240Thr
ENST00000584322.2:c.1226G>C	ENSP00000463272.2:p.Ser409Thr
ENST00000682066.1:c.719G>C	ENSP00000507191.1:p.Ser240Thr
ENST00000682453.1:c.1226G>C	ENSP00000506943.1:p.Ser409Thr
ENST00000682477.1:c.1226G>C	ENSP00000507075.1:p.Ser409Thr
ENST00000682589.1:n.2967G>C
ENST00000682611.1:c.719G>C	ENSP00000508326.1:p.Ser240Thr
ENST00000682755.1:c.1004G>C	ENSP00000507660.1:p.Ser335Thr
ENST00000682989.1:c.1226G>C	ENSP00000507786.1:p.Ser409Thr
ENST00000683039.1:c.1226G>C	ENSP00000508303.1:p.Ser409Thr
ENST00000683235.1:c.1226G>C	ENSP00000507646.1:p.Ser409Thr
ENST00000683381.1:c.1226G>C	ENSP00000508184.1:p.Ser409Thr
ENST00000683692.1:c.804G>C	ENSP00000507964.1:n.804G>C
ENST00000684584.1:c.719G>C	ENSP00000508044.1:p.Ser240Thr
ENST00000259008.7:c.1226G>C MANE Select	ENSP00000259008.2:p.Ser409Thr
ENST00000259008.6:c.1226G>C	ENSP00000259008.2:p.Ser409Thr
ENST00000577598.5:c.1226G>C	ENSP00000464654.1:p.Ser409Thr
NM_032043.2:c.1226G>C , LRG_300t1:c.1226G>C	NP_114432.2:p.Ser409Thr
XM_011525332.1:c.1226G>C	XP_011523634.1:p.Ser409Thr
XM_011525333.1:c.1226G>C	XP_011523635.1:p.Ser409Thr
XM_011525334.1:c.1226G>C	XP_011523636.1:p.Ser409Thr
XM_011525335.1:c.1226G>C	XP_011523637.1:p.Ser409Thr
XM_011525336.1:c.1226G>C	XP_011523638.1:p.Ser409Thr
XM_011525337.1:c.1226G>C	XP_011523639.1:p.Ser409Thr
XM_011525338.1:c.743G>C	XP_011523640.1:p.Ser248Thr
XM_011525339.1:c.1226G>C	XP_011523641.1:p.Ser409Thr
XM_011525340.1:c.1226G>C	XP_011523642.1:p.Ser409Thr
XM_011525341.1:c.1226G>C	XP_011523643.1:p.Ser409Thr
XM_011525332.3:c.1226G>C	XP_011523634.1:p.Ser409Thr
XM_011525333.3:c.1226G>C	XP_011523635.1:p.Ser409Thr
XM_011525334.2:c.1226G>C	XP_011523636.1:p.Ser409Thr
XM_011525335.3:c.1226G>C	XP_011523637.1:p.Ser409Thr
XM_011525336.2:c.1226G>C	XP_011523638.1:p.Ser409Thr
XM_011525337.2:c.1226G>C	XP_011523639.1:p.Ser409Thr
XM_011525338.2:c.743G>C	XP_011523640.1:p.Ser248Thr
XM_011525339.3:c.1226G>C	XP_011523641.1:p.Ser409Thr
XM_011525340.3:c.1226G>C	XP_011523642.1:p.Ser409Thr
XM_011525341.3:c.1226G>C	XP_011523643.1:p.Ser409Thr
XM_017025200.1:c.743G>C	XP_016880689.1:p.Ser248Thr
XM_017025201.1:c.683G>C	XP_016880690.1:p.Ser228Thr
NM_032043.3:c.1226G>C MANE Select	NP_114432.2:p.Ser409Thr