Canonical Allele Identifier: CA400481393

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59763267T>G (hg19) ; chr17:g.61685906T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685906T>G , CM000679.2:g.61685906T>G	GRCh38
NC_000017.10:g.59763267T>G , CM000679.1:g.59763267T>G	GRCh37
NC_000017.9:g.57118049T>G	NCBI36
NG_007409.2:g.182654A>C , LRG_300:g.182654A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682066.1:c.2965A>C	ENSP00000507191.1:n.2965A>C
ENST00000682073.1:n.1575A>C
ENST00000682433.1:n.1914A>C
ENST00000682453.1:c.2835A>C	ENSP00000506943.1:p.Glu945Asp
ENST00000682477.1:c.*2261A>C	ENSP00000507075.1:n.*2261A>C
ENST00000682589.1:n.8712A>C
ENST00000682755.1:c.2613A>C	ENSP00000507660.1:p.Glu871Asp
ENST00000682989.1:c.2610-1766A>C	ENSP00000507786.1:n.2610-1766A>C
ENST00000683039.1:c.2835A>C	ENSP00000508303.1:p.Glu945Asp
ENST00000683235.1:c.*250A>C	ENSP00000507646.1:n.*250A>C
ENST00000683535.1:n.965A>C
ENST00000684471.1:n.1248A>C
ENST00000684584.1:c.2069-1766A>C	ENSP00000508044.1:n.2069-1766A>C
ENST00000684626.1:n.1081A>C
ENST00000684769.1:c.1025A>C	ENSP00000507691.1:n.1025A>C
ENST00000259008.7:c.2835A>C MANE Select	ENSP00000259008.2:p.Glu945Asp
ENST00000259008.6:c.2835A>C	ENSP00000259008.2:p.Glu945Asp
ENST00000577598.5:c.2835A>C	ENSP00000464654.1:p.Glu945Asp
NM_032043.2:c.2835A>C , LRG_300t1:c.2835A>C	NP_114432.2:p.Glu945Asp
XM_011525332.1:c.2895A>C	XP_011523634.1:p.Glu965Asp
XM_011525333.1:c.2895A>C	XP_011523635.1:p.Glu965Asp
XM_011525334.1:c.2895A>C	XP_011523636.1:p.Glu965Asp
XM_011525335.1:c.2835A>C	XP_011523637.1:p.Glu945Asp
XM_011525336.1:c.2775A>C	XP_011523638.1:p.Glu925Asp
XM_011525337.1:c.2694A>C	XP_011523639.1:p.Glu898Asp
XM_011525338.1:c.2412A>C	XP_011523640.1:p.Glu804Asp
XM_011525332.3:c.2895A>C	XP_011523634.1:p.Glu965Asp
XM_011525333.3:c.2895A>C	XP_011523635.1:p.Glu965Asp
XM_011525334.2:c.2895A>C	XP_011523636.1:p.Glu965Asp
XM_011525335.3:c.2835A>C	XP_011523637.1:p.Glu945Asp
XM_011525336.2:c.2775A>C	XP_011523638.1:p.Glu925Asp
XM_011525337.2:c.2694A>C	XP_011523639.1:p.Glu898Asp
XM_011525338.2:c.2412A>C	XP_011523640.1:p.Glu804Asp
XM_017025200.1:c.2352A>C	XP_016880689.1:p.Glu784Asp
XM_017025201.1:c.2352A>C	XP_016880690.1:p.Glu784Asp
XM_017025202.1:c.981A>C	XP_016880691.1:p.Glu327Asp
XM_017025203.1:c.981A>C	XP_016880692.1:p.Glu327Asp
NM_032043.3:c.2835A>C MANE Select	NP_114432.2:p.Glu945Asp