Canonical Allele Identifier: CA400478363

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 841198
• ClinVar RCV Id: RCV001043372 ; RCV002339218
• dbSNP Id: rs2061303001
• gnomAD v4: 17-61683508-C-G
• MyVariant Identifiers: chr17:g.59760869C>G (hg19) ; chr17:g.61683508C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683508C>G , CM000679.2:g.61683508C>G	GRCh38
NC_000017.10:g.59760869C>G , CM000679.1:g.59760869C>G	GRCh37
NC_000017.9:g.57115651C>G	NCBI36
NG_007409.2:g.185052G>C , LRG_300:g.185052G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2278G>C
ENST00000682453.1:c.3538G>C	ENSP00000506943.1:p.Asp1180His
ENST00000682477.1:c.*2964G>C	ENSP00000507075.1:n.*2964G>C
ENST00000682589.1:n.9415G>C
ENST00000682755.1:c.3316G>C	ENSP00000507660.1:p.Asp1106His
ENST00000682989.1:c.*629G>C	ENSP00000507786.1:n.*629G>C
ENST00000683039.1:c.3538G>C	ENSP00000508303.1:p.Asp1180His
ENST00000683235.1:c.*953G>C	ENSP00000507646.1:n.*953G>C
ENST00000683535.1:n.1668G>C
ENST00000684584.1:c.2701G>C	ENSP00000508044.1:p.Asp901His
ENST00000684626.1:n.1784G>C
ENST00000684769.1:c.1728G>C	ENSP00000507691.1:n.1728G>C
ENST00000259008.7:c.3538G>C MANE Select	ENSP00000259008.2:p.Asp1180His
ENST00000259008.6:c.3538G>C	ENSP00000259008.2:p.Asp1180His
NM_032043.2:c.3538G>C , LRG_300t1:c.3538G>C	NP_114432.2:p.Asp1180His
XM_011525332.1:c.3598G>C	XP_011523634.1:p.Asp1200His
XM_011525333.1:c.3598G>C	XP_011523635.1:p.Asp1200His
XM_011525334.1:c.3598G>C	XP_011523636.1:p.Asp1200His
XM_011525335.1:c.3538G>C	XP_011523637.1:p.Asp1180His
XM_011525336.1:c.3478G>C	XP_011523638.1:p.Asp1160His
XM_011525337.1:c.3397G>C	XP_011523639.1:p.Asp1133His
XM_011525338.1:c.3115G>C	XP_011523640.1:p.Asp1039His
XM_011525332.3:c.3598G>C	XP_011523634.1:p.Asp1200His
XM_011525333.3:c.3598G>C	XP_011523635.1:p.Asp1200His
XM_011525334.2:c.3598G>C	XP_011523636.1:p.Asp1200His
XM_011525335.3:c.3538G>C	XP_011523637.1:p.Asp1180His
XM_011525336.2:c.3478G>C	XP_011523638.1:p.Asp1160His
XM_011525337.2:c.3397G>C	XP_011523639.1:p.Asp1133His
XM_011525338.2:c.3115G>C	XP_011523640.1:p.Asp1039His
XM_017025200.1:c.3055G>C	XP_016880689.1:p.Asp1019His
XM_017025201.1:c.3055G>C	XP_016880690.1:p.Asp1019His
XM_017025202.1:c.1684G>C	XP_016880691.1:p.Asp562His
XM_017025203.1:c.1684G>C	XP_016880692.1:p.Asp562His
NM_032043.3:c.3538G>C MANE Select	NP_114432.2:p.Asp1180His