Canonical Allele Identifier: CA400478625

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 823816
• ClinVar RCV Id: RCV001020393 ; RCV001860985
• dbSNP Id: rs368610199
• MyVariant Identifiers: chr17:g.59760932C>G (hg19) ; chr17:g.61683571C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683571C>G , CM000679.2:g.61683571C>G	GRCh38
NC_000017.10:g.59760932C>G , CM000679.1:g.59760932C>G	GRCh37
NC_000017.9:g.57115714C>G	NCBI36
NG_007409.2:g.184989G>C , LRG_300:g.184989G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2215G>C
ENST00000682453.1:c.3475G>C	ENSP00000506943.1:p.Ala1159Pro
ENST00000682477.1:c.*2901G>C	ENSP00000507075.1:n.*2901G>C
ENST00000682589.1:n.9352G>C
ENST00000682755.1:c.3253G>C	ENSP00000507660.1:p.Ala1085Pro
ENST00000682989.1:c.*566G>C	ENSP00000507786.1:n.*566G>C
ENST00000683039.1:c.3475G>C	ENSP00000508303.1:p.Ala1159Pro
ENST00000683235.1:c.*890G>C	ENSP00000507646.1:n.*890G>C
ENST00000683535.1:n.1605G>C
ENST00000684584.1:c.2638G>C	ENSP00000508044.1:p.Ala880Pro
ENST00000684626.1:n.1721G>C
ENST00000684769.1:c.1665G>C	ENSP00000507691.1:n.1665G>C
ENST00000259008.7:c.3475G>C MANE Select	ENSP00000259008.2:p.Ala1159Pro
ENST00000259008.6:c.3475G>C	ENSP00000259008.2:p.Ala1159Pro
NM_032043.2:c.3475G>C , LRG_300t1:c.3475G>C	NP_114432.2:p.Ala1159Pro
XM_011525332.1:c.3535G>C	XP_011523634.1:p.Ala1179Pro
XM_011525333.1:c.3535G>C	XP_011523635.1:p.Ala1179Pro
XM_011525334.1:c.3535G>C	XP_011523636.1:p.Ala1179Pro
XM_011525335.1:c.3475G>C	XP_011523637.1:p.Ala1159Pro
XM_011525336.1:c.3415G>C	XP_011523638.1:p.Ala1139Pro
XM_011525337.1:c.3334G>C	XP_011523639.1:p.Ala1112Pro
XM_011525338.1:c.3052G>C	XP_011523640.1:p.Ala1018Pro
XM_011525332.3:c.3535G>C	XP_011523634.1:p.Ala1179Pro
XM_011525333.3:c.3535G>C	XP_011523635.1:p.Ala1179Pro
XM_011525334.2:c.3535G>C	XP_011523636.1:p.Ala1179Pro
XM_011525335.3:c.3475G>C	XP_011523637.1:p.Ala1159Pro
XM_011525336.2:c.3415G>C	XP_011523638.1:p.Ala1139Pro
XM_011525337.2:c.3334G>C	XP_011523639.1:p.Ala1112Pro
XM_011525338.2:c.3052G>C	XP_011523640.1:p.Ala1018Pro
XM_017025200.1:c.2992G>C	XP_016880689.1:p.Ala998Pro
XM_017025201.1:c.2992G>C	XP_016880690.1:p.Ala998Pro
XM_017025202.1:c.1621G>C	XP_016880691.1:p.Ala541Pro
XM_017025203.1:c.1621G>C	XP_016880692.1:p.Ala541Pro
NM_032043.3:c.3475G>C MANE Select	NP_114432.2:p.Ala1159Pro