Canonical Allele Identifier: CA400485913

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 998759
• ClinVar RCV Id: RCV001294659
• dbSNP Id: rs2078971287
• MyVariant Identifiers: chr17:g.59938816T>C (hg19) ; chr17:g.61861455T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61861455T>C , CM000679.2:g.61861455T>C	GRCh38
NC_000017.10:g.59938816T>C , CM000679.1:g.59938816T>C	GRCh37
NC_000017.9:g.57293598T>C	NCBI36
NG_007409.2:g.7105A>G , LRG_300:g.7105A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000577913.2:c.85A>G	ENSP00000462274.2:p.Met29Val
ENST00000584322.2:c.85A>G	ENSP00000463272.2:p.Met29Val
ENST00000682369.1:c.85A>G	ENSP00000507450.1:p.Met29Val
ENST00000682453.1:c.85A>G	ENSP00000506943.1:p.Met29Val
ENST00000682477.1:c.85A>G	ENSP00000507075.1:p.Met29Val
ENST00000682589.1:n.1826A>G
ENST00000682755.1:c.85A>G	ENSP00000507660.1:p.Met29Val
ENST00000682989.1:c.85A>G	ENSP00000507786.1:p.Met29Val
ENST00000683039.1:c.85A>G	ENSP00000508303.1:p.Met29Val
ENST00000683235.1:c.85A>G	ENSP00000507646.1:p.Met29Val
ENST00000683381.1:c.85A>G	ENSP00000508184.1:p.Met29Val
ENST00000683672.1:c.-93+1829A>G	ENSP00000506781.1:n.-93+1829A>G
ENST00000259008.7:c.85A>G MANE Select	ENSP00000259008.2:p.Met29Val
ENST00000259008.6:c.85A>G	ENSP00000259008.2:p.Met29Val
ENST00000577598.5:c.85A>G	ENSP00000464654.1:p.Met29Val
ENST00000577913.1:c.85A>G	ENSP00000462274.1:p.Met29Val
NM_032043.2:c.85A>G , LRG_300t1:c.85A>G	NP_114432.2:p.Met29Val
XM_011525332.1:c.85A>G	XP_011523634.1:p.Met29Val
XM_011525333.1:c.85A>G	XP_011523635.1:p.Met29Val
XM_011525334.1:c.85A>G	XP_011523636.1:p.Met29Val
XM_011525335.1:c.85A>G	XP_011523637.1:p.Met29Val
XM_011525336.1:c.85A>G	XP_011523638.1:p.Met29Val
XM_011525337.1:c.85A>G	XP_011523639.1:p.Met29Val
XM_011525339.1:c.85A>G	XP_011523641.1:p.Met29Val
XM_011525340.1:c.85A>G	XP_011523642.1:p.Met29Val
XM_011525341.1:c.85A>G	XP_011523643.1:p.Met29Val
XM_011525332.3:c.85A>G	XP_011523634.1:p.Met29Val
XM_011525333.3:c.85A>G	XP_011523635.1:p.Met29Val
XM_011525334.2:c.85A>G	XP_011523636.1:p.Met29Val
XM_011525335.3:c.85A>G	XP_011523637.1:p.Met29Val
XM_011525336.2:c.85A>G	XP_011523638.1:p.Met29Val
XM_011525337.2:c.85A>G	XP_011523639.1:p.Met29Val
XM_011525339.3:c.85A>G	XP_011523641.1:p.Met29Val
XM_011525340.3:c.85A>G	XP_011523642.1:p.Met29Val
XM_011525341.3:c.85A>G	XP_011523643.1:p.Met29Val
NM_032043.3:c.85A>G MANE Select	NP_114432.2:p.Met29Val