Canonical Allele Identifier: CA400481341

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59763256G>C (hg19) ; chr17:g.61685895G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685895G>C , CM000679.2:g.61685895G>C	GRCh38
NC_000017.10:g.59763256G>C , CM000679.1:g.59763256G>C	GRCh37
NC_000017.9:g.57118038G>C	NCBI36
NG_007409.2:g.182665C>G , LRG_300:g.182665C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2976C>G	ENSP00000507191.1:n.2976C>G
ENST00000682073.1:n.1586C>G
ENST00000682433.1:n.1925C>G
ENST00000682453.1:c.2846C>G	ENSP00000506943.1:p.Pro949Arg
ENST00000682477.1:c.*2272C>G	ENSP00000507075.1:n.*2272C>G
ENST00000682589.1:n.8723C>G
ENST00000682755.1:c.2624C>G	ENSP00000507660.1:p.Pro875Arg
ENST00000682989.1:c.2610-1755C>G	ENSP00000507786.1:n.2610-1755C>G
ENST00000683039.1:c.2846C>G	ENSP00000508303.1:p.Pro949Arg
ENST00000683235.1:c.*261C>G	ENSP00000507646.1:n.*261C>G
ENST00000683535.1:n.976C>G
ENST00000684471.1:n.1259C>G
ENST00000684584.1:c.2069-1755C>G	ENSP00000508044.1:n.2069-1755C>G
ENST00000684626.1:n.1092C>G
ENST00000684769.1:c.1036C>G	ENSP00000507691.1:n.1036C>G
ENST00000259008.7:c.2846C>G MANE Select	ENSP00000259008.2:p.Pro949Arg
ENST00000259008.6:c.2846C>G	ENSP00000259008.2:p.Pro949Arg
ENST00000577598.5:c.2846C>G	ENSP00000464654.1:p.Pro949Arg
NM_032043.2:c.2846C>G , LRG_300t1:c.2846C>G	NP_114432.2:p.Pro949Arg
XM_011525332.1:c.2906C>G	XP_011523634.1:p.Pro969Arg
XM_011525333.1:c.2906C>G	XP_011523635.1:p.Pro969Arg
XM_011525334.1:c.2906C>G	XP_011523636.1:p.Pro969Arg
XM_011525335.1:c.2846C>G	XP_011523637.1:p.Pro949Arg
XM_011525336.1:c.2786C>G	XP_011523638.1:p.Pro929Arg
XM_011525337.1:c.2705C>G	XP_011523639.1:p.Pro902Arg
XM_011525338.1:c.2423C>G	XP_011523640.1:p.Pro808Arg
XM_011525332.3:c.2906C>G	XP_011523634.1:p.Pro969Arg
XM_011525333.3:c.2906C>G	XP_011523635.1:p.Pro969Arg
XM_011525334.2:c.2906C>G	XP_011523636.1:p.Pro969Arg
XM_011525335.3:c.2846C>G	XP_011523637.1:p.Pro949Arg
XM_011525336.2:c.2786C>G	XP_011523638.1:p.Pro929Arg
XM_011525337.2:c.2705C>G	XP_011523639.1:p.Pro902Arg
XM_011525338.2:c.2423C>G	XP_011523640.1:p.Pro808Arg
XM_017025200.1:c.2363C>G	XP_016880689.1:p.Pro788Arg
XM_017025201.1:c.2363C>G	XP_016880690.1:p.Pro788Arg
XM_017025202.1:c.992C>G	XP_016880691.1:p.Pro331Arg
XM_017025203.1:c.992C>G	XP_016880692.1:p.Pro331Arg
NM_032043.3:c.2846C>G MANE Select	NP_114432.2:p.Pro949Arg