Canonical Allele Identifier: CA400485634

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 483196
• ClinVar RCV Id: RCV000563712 ; RCV000693188 ; RCV001755942
• dbSNP Id: rs1555617934
• gnomAD v4: 17-61857232-C-A
• MyVariant Identifiers: chr17:g.59934593C>A (hg19) ; chr17:g.61857232C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61857232C>A , CM000679.2:g.61857232C>A	GRCh38
NC_000017.10:g.59934593C>A , CM000679.1:g.59934593C>A	GRCh37
NC_000017.9:g.57289375C>A	NCBI36
NG_007409.2:g.11328G>T , LRG_300:g.11328G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000577913.2:c.206-1G>T	ENSP00000462274.2:n.206-1G>T
ENST00000584322.2:c.206-1G>T	ENSP00000463272.2:n.206-1G>T
ENST00000682369.1:c.206-1G>T	ENSP00000507450.1:n.206-1G>T
ENST00000682453.1:c.206-1G>T	ENSP00000506943.1:n.206-1G>T
ENST00000682477.1:c.206-1G>T	ENSP00000507075.1:n.206-1G>T
ENST00000682589.1:n.1947-1G>T
ENST00000682755.1:c.206-1G>T	ENSP00000507660.1:n.206-1G>T
ENST00000682989.1:c.206-1G>T	ENSP00000507786.1:n.206-1G>T
ENST00000683039.1:c.206-1G>T	ENSP00000508303.1:n.206-1G>T
ENST00000683235.1:c.206-1G>T	ENSP00000507646.1:n.206-1G>T
ENST00000683381.1:c.206-1G>T	ENSP00000508184.1:n.206-1G>T
ENST00000683672.1:c.-92-1G>T	ENSP00000506781.1:n.-92-1G>T
ENST00000259008.7:c.206-1G>T MANE Select	ENSP00000259008.2:n.206-1G>T
ENST00000259008.6:c.206-1G>T	ENSP00000259008.2:n.206-1G>T
ENST00000577598.5:c.206-1G>T	ENSP00000464654.1:n.206-1G>T
ENST00000577913.1:c.206-1G>T	ENSP00000462274.1:n.206-1G>T
NM_032043.2:c.206-1G>T , LRG_300t1:c.206-1G>T	NP_114432.2:n.206-1G>T
XM_011525332.1:c.206-1G>T	XP_011523634.1:n.206-1G>T
XM_011525333.1:c.206-1G>T	XP_011523635.1:n.206-1G>T
XM_011525334.1:c.206-1G>T	XP_011523636.1:n.206-1G>T
XM_011525335.1:c.206-1G>T	XP_011523637.1:n.206-1G>T
XM_011525336.1:c.206-1G>T	XP_011523638.1:n.206-1G>T
XM_011525337.1:c.206-1G>T	XP_011523639.1:n.206-1G>T
XM_011525339.1:c.206-1G>T	XP_011523641.1:n.206-1G>T
XM_011525340.1:c.206-1G>T	XP_011523642.1:n.206-1G>T
XM_011525341.1:c.206-1G>T	XP_011523643.1:n.206-1G>T
XM_011525332.3:c.206-1G>T	XP_011523634.1:n.206-1G>T
XM_011525333.3:c.206-1G>T	XP_011523635.1:n.206-1G>T
XM_011525334.2:c.206-1G>T	XP_011523636.1:n.206-1G>T
XM_011525335.3:c.206-1G>T	XP_011523637.1:n.206-1G>T
XM_011525336.2:c.206-1G>T	XP_011523638.1:n.206-1G>T
XM_011525337.2:c.206-1G>T	XP_011523639.1:n.206-1G>T
XM_011525339.3:c.206-1G>T	XP_011523641.1:n.206-1G>T
XM_011525340.3:c.206-1G>T	XP_011523642.1:n.206-1G>T
XM_011525341.3:c.206-1G>T	XP_011523643.1:n.206-1G>T
NM_032043.3:c.206-1G>T MANE Select	NP_114432.2:n.206-1G>T