Canonical Allele Identifier: CA400479003

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 491467
• ClinVar RCV Id: RCV000584290 ; RCV001065231
• dbSNP Id: rs1555572697
• gnomAD v4: 17-61683734-T-A
• MyVariant Identifiers: chr17:g.59761095T>A (hg19) ; chr17:g.61683734T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683734T>A , CM000679.2:g.61683734T>A	GRCh38
NC_000017.10:g.59761095T>A , CM000679.1:g.59761095T>A	GRCh37
NC_000017.9:g.57115877T>A	NCBI36
NG_007409.2:g.184826A>T , LRG_300:g.184826A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2052A>T
ENST00000682453.1:c.3312A>T	ENSP00000506943.1:p.Glu1104Asp
ENST00000682477.1:c.*2738A>T	ENSP00000507075.1:n.*2738A>T
ENST00000682589.1:n.9189A>T
ENST00000682755.1:c.3090A>T	ENSP00000507660.1:p.Glu1030Asp
ENST00000682989.1:c.*403A>T	ENSP00000507786.1:n.*403A>T
ENST00000683039.1:c.3312A>T	ENSP00000508303.1:p.Glu1104Asp
ENST00000683235.1:c.*727A>T	ENSP00000507646.1:n.*727A>T
ENST00000683535.1:n.1442A>T
ENST00000684584.1:c.2475A>T	ENSP00000508044.1:p.Glu825Asp
ENST00000684626.1:n.1558A>T
ENST00000684769.1:c.1502A>T	ENSP00000507691.1:n.1502A>T
ENST00000259008.7:c.3312A>T MANE Select	ENSP00000259008.2:p.Glu1104Asp
ENST00000259008.6:c.3312A>T	ENSP00000259008.2:p.Glu1104Asp
NM_032043.2:c.3312A>T , LRG_300t1:c.3312A>T	NP_114432.2:p.Glu1104Asp
XM_011525332.1:c.3372A>T	XP_011523634.1:p.Glu1124Asp
XM_011525333.1:c.3372A>T	XP_011523635.1:p.Glu1124Asp
XM_011525334.1:c.3372A>T	XP_011523636.1:p.Glu1124Asp
XM_011525335.1:c.3312A>T	XP_011523637.1:p.Glu1104Asp
XM_011525336.1:c.3252A>T	XP_011523638.1:p.Glu1084Asp
XM_011525337.1:c.3171A>T	XP_011523639.1:p.Glu1057Asp
XM_011525338.1:c.2889A>T	XP_011523640.1:p.Glu963Asp
XM_011525332.3:c.3372A>T	XP_011523634.1:p.Glu1124Asp
XM_011525333.3:c.3372A>T	XP_011523635.1:p.Glu1124Asp
XM_011525334.2:c.3372A>T	XP_011523636.1:p.Glu1124Asp
XM_011525335.3:c.3312A>T	XP_011523637.1:p.Glu1104Asp
XM_011525336.2:c.3252A>T	XP_011523638.1:p.Glu1084Asp
XM_011525337.2:c.3171A>T	XP_011523639.1:p.Glu1057Asp
XM_011525338.2:c.2889A>T	XP_011523640.1:p.Glu963Asp
XM_017025200.1:c.2829A>T	XP_016880689.1:p.Glu943Asp
XM_017025201.1:c.2829A>T	XP_016880690.1:p.Glu943Asp
XM_017025202.1:c.1458A>T	XP_016880691.1:p.Glu486Asp
XM_017025203.1:c.1458A>T	XP_016880692.1:p.Glu486Asp
NM_032043.3:c.3312A>T MANE Select	NP_114432.2:p.Glu1104Asp