Canonical Allele Identifier: CA400479255

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 1440286
• ClinVar RCV Id: RCV001967633
• dbSNP Id: rs1219988835
• gnomAD v2: 17-59761186-A-G
• gnomAD v4: 17-61683825-A-G
• MyVariant Identifiers: chr17:g.59761186A>G (hg19) ; chr17:g.61683825A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683825A>G , CM000679.2:g.61683825A>G	GRCh38
NC_000017.10:g.59761186A>G , CM000679.1:g.59761186A>G	GRCh37
NC_000017.9:g.57115968A>G	NCBI36
NG_007409.2:g.184735T>C , LRG_300:g.184735T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1961T>C
ENST00000682453.1:c.3221T>C	ENSP00000506943.1:p.Ile1074Thr
ENST00000682477.1:c.*2647T>C	ENSP00000507075.1:n.*2647T>C
ENST00000682589.1:n.9098T>C
ENST00000682755.1:c.2999T>C	ENSP00000507660.1:p.Ile1000Thr
ENST00000682989.1:c.*312T>C	ENSP00000507786.1:n.*312T>C
ENST00000683039.1:c.3221T>C	ENSP00000508303.1:p.Ile1074Thr
ENST00000683235.1:c.*636T>C	ENSP00000507646.1:n.*636T>C
ENST00000683535.1:n.1351T>C
ENST00000684584.1:c.2384T>C	ENSP00000508044.1:p.Ile795Thr
ENST00000684626.1:n.1467T>C
ENST00000684769.1:c.1411T>C	ENSP00000507691.1:n.1411T>C
ENST00000259008.7:c.3221T>C MANE Select	ENSP00000259008.2:p.Ile1074Thr
ENST00000259008.6:c.3221T>C	ENSP00000259008.2:p.Ile1074Thr
NM_032043.2:c.3221T>C , LRG_300t1:c.3221T>C	NP_114432.2:p.Ile1074Thr
XM_011525332.1:c.3281T>C	XP_011523634.1:p.Ile1094Thr
XM_011525333.1:c.3281T>C	XP_011523635.1:p.Ile1094Thr
XM_011525334.1:c.3281T>C	XP_011523636.1:p.Ile1094Thr
XM_011525335.1:c.3221T>C	XP_011523637.1:p.Ile1074Thr
XM_011525336.1:c.3161T>C	XP_011523638.1:p.Ile1054Thr
XM_011525337.1:c.3080T>C	XP_011523639.1:p.Ile1027Thr
XM_011525338.1:c.2798T>C	XP_011523640.1:p.Ile933Thr
XM_011525332.3:c.3281T>C	XP_011523634.1:p.Ile1094Thr
XM_011525333.3:c.3281T>C	XP_011523635.1:p.Ile1094Thr
XM_011525334.2:c.3281T>C	XP_011523636.1:p.Ile1094Thr
XM_011525335.3:c.3221T>C	XP_011523637.1:p.Ile1074Thr
XM_011525336.2:c.3161T>C	XP_011523638.1:p.Ile1054Thr
XM_011525337.2:c.3080T>C	XP_011523639.1:p.Ile1027Thr
XM_011525338.2:c.2798T>C	XP_011523640.1:p.Ile933Thr
XM_017025200.1:c.2738T>C	XP_016880689.1:p.Ile913Thr
XM_017025201.1:c.2738T>C	XP_016880690.1:p.Ile913Thr
XM_017025202.1:c.1367T>C	XP_016880691.1:p.Ile456Thr
XM_017025203.1:c.1367T>C	XP_016880692.1:p.Ile456Thr
NM_032043.3:c.3221T>C MANE Select	NP_114432.2:p.Ile1074Thr