Canonical Allele Identifier: CA400478954

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59761071A>C (hg19) ; chr17:g.61683710A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683710A>C , CM000679.2:g.61683710A>C	GRCh38
NC_000017.10:g.59761071A>C , CM000679.1:g.59761071A>C	GRCh37
NC_000017.9:g.57115853A>C	NCBI36
NG_007409.2:g.184850T>G , LRG_300:g.184850T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2076T>G
ENST00000682453.1:c.3336T>G	ENSP00000506943.1:p.Asp1112Glu
ENST00000682477.1:c.*2762T>G	ENSP00000507075.1:n.*2762T>G
ENST00000682589.1:n.9213T>G
ENST00000682755.1:c.3114T>G	ENSP00000507660.1:p.Asp1038Glu
ENST00000682989.1:c.*427T>G	ENSP00000507786.1:n.*427T>G
ENST00000683039.1:c.3336T>G	ENSP00000508303.1:p.Asp1112Glu
ENST00000683235.1:c.*751T>G	ENSP00000507646.1:n.*751T>G
ENST00000683535.1:n.1466T>G
ENST00000684584.1:c.2499T>G	ENSP00000508044.1:p.Asp833Glu
ENST00000684626.1:n.1582T>G
ENST00000684769.1:c.1526T>G	ENSP00000507691.1:n.1526T>G
ENST00000259008.7:c.3336T>G MANE Select	ENSP00000259008.2:p.Asp1112Glu
ENST00000259008.6:c.3336T>G	ENSP00000259008.2:p.Asp1112Glu
NM_032043.2:c.3336T>G , LRG_300t1:c.3336T>G	NP_114432.2:p.Asp1112Glu
XM_011525332.1:c.3396T>G	XP_011523634.1:p.Asp1132Glu
XM_011525333.1:c.3396T>G	XP_011523635.1:p.Asp1132Glu
XM_011525334.1:c.3396T>G	XP_011523636.1:p.Asp1132Glu
XM_011525335.1:c.3336T>G	XP_011523637.1:p.Asp1112Glu
XM_011525336.1:c.3276T>G	XP_011523638.1:p.Asp1092Glu
XM_011525337.1:c.3195T>G	XP_011523639.1:p.Asp1065Glu
XM_011525338.1:c.2913T>G	XP_011523640.1:p.Asp971Glu
XM_011525332.3:c.3396T>G	XP_011523634.1:p.Asp1132Glu
XM_011525333.3:c.3396T>G	XP_011523635.1:p.Asp1132Glu
XM_011525334.2:c.3396T>G	XP_011523636.1:p.Asp1132Glu
XM_011525335.3:c.3336T>G	XP_011523637.1:p.Asp1112Glu
XM_011525336.2:c.3276T>G	XP_011523638.1:p.Asp1092Glu
XM_011525337.2:c.3195T>G	XP_011523639.1:p.Asp1065Glu
XM_011525338.2:c.2913T>G	XP_011523640.1:p.Asp971Glu
XM_017025200.1:c.2853T>G	XP_016880689.1:p.Asp951Glu
XM_017025201.1:c.2853T>G	XP_016880690.1:p.Asp951Glu
XM_017025202.1:c.1482T>G	XP_016880691.1:p.Asp494Glu
XM_017025203.1:c.1482T>G	XP_016880692.1:p.Asp494Glu
NM_032043.3:c.3336T>G MANE Select	NP_114432.2:p.Asp1112Glu