Canonical Allele Identifier: CA400479887

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144089694
• MyVariant Identifiers: chr17:g.59761345G>T (hg19) ; chr17:g.61683984G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683984G>T , CM000679.2:g.61683984G>T	GRCh38
NC_000017.10:g.59761345G>T , CM000679.1:g.59761345G>T	GRCh37
NC_000017.9:g.57116127G>T	NCBI36
NG_007409.2:g.184576C>A , LRG_300:g.184576C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682073.1:n.1802C>A
ENST00000682453.1:c.3062C>A	ENSP00000506943.1:p.Pro1021His
ENST00000682477.1:c.*2488C>A	ENSP00000507075.1:n.*2488C>A
ENST00000682589.1:n.8939C>A
ENST00000682755.1:c.2840C>A	ENSP00000507660.1:p.Pro947His
ENST00000682989.1:c.*153C>A	ENSP00000507786.1:n.*153C>A
ENST00000683039.1:c.3062C>A	ENSP00000508303.1:p.Pro1021His
ENST00000683235.1:c.*477C>A	ENSP00000507646.1:n.*477C>A
ENST00000683535.1:n.1192C>A
ENST00000684584.1:c.2225C>A	ENSP00000508044.1:p.Pro742His
ENST00000684626.1:n.1308C>A
ENST00000684769.1:c.1252C>A	ENSP00000507691.1:n.1252C>A
ENST00000259008.7:c.3062C>A MANE Select	ENSP00000259008.2:p.Pro1021His
ENST00000259008.6:c.3062C>A	ENSP00000259008.2:p.Pro1021His
NM_032043.2:c.3062C>A , LRG_300t1:c.3062C>A	NP_114432.2:p.Pro1021His
XM_011525332.1:c.3122C>A	XP_011523634.1:p.Pro1041His
XM_011525333.1:c.3122C>A	XP_011523635.1:p.Pro1041His
XM_011525334.1:c.3122C>A	XP_011523636.1:p.Pro1041His
XM_011525335.1:c.3062C>A	XP_011523637.1:p.Pro1021His
XM_011525336.1:c.3002C>A	XP_011523638.1:p.Pro1001His
XM_011525337.1:c.2921C>A	XP_011523639.1:p.Pro974His
XM_011525338.1:c.2639C>A	XP_011523640.1:p.Pro880His
XM_011525332.3:c.3122C>A	XP_011523634.1:p.Pro1041His
XM_011525333.3:c.3122C>A	XP_011523635.1:p.Pro1041His
XM_011525334.2:c.3122C>A	XP_011523636.1:p.Pro1041His
XM_011525335.3:c.3062C>A	XP_011523637.1:p.Pro1021His
XM_011525336.2:c.3002C>A	XP_011523638.1:p.Pro1001His
XM_011525337.2:c.2921C>A	XP_011523639.1:p.Pro974His
XM_011525338.2:c.2639C>A	XP_011523640.1:p.Pro880His
XM_017025200.1:c.2579C>A	XP_016880689.1:p.Pro860His
XM_017025201.1:c.2579C>A	XP_016880690.1:p.Pro860His
XM_017025202.1:c.1208C>A	XP_016880691.1:p.Pro403His
XM_017025203.1:c.1208C>A	XP_016880692.1:p.Pro403His
NM_032043.3:c.3062C>A MANE Select	NP_114432.2:p.Pro1021His