Canonical Allele Identifier: CA400478722

Gene: BRIP1

Linked Data

• dbSNP Id: rs1258403817
• MyVariant Identifiers: chr17:g.59760968T>A (hg19) ; chr17:g.61683607T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683607T>A , CM000679.2:g.61683607T>A	GRCh38
NC_000017.10:g.59760968T>A , CM000679.1:g.59760968T>A	GRCh37
NC_000017.9:g.57115750T>A	NCBI36
NG_007409.2:g.184953A>T , LRG_300:g.184953A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2179A>T
ENST00000682453.1:c.3439A>T	ENSP00000506943.1:p.Asn1147Tyr
ENST00000682477.1:c.*2865A>T	ENSP00000507075.1:n.*2865A>T
ENST00000682589.1:n.9316A>T
ENST00000682755.1:c.3217A>T	ENSP00000507660.1:p.Asn1073Tyr
ENST00000682989.1:c.*530A>T	ENSP00000507786.1:n.*530A>T
ENST00000683039.1:c.3439A>T	ENSP00000508303.1:p.Asn1147Tyr
ENST00000683235.1:c.*854A>T	ENSP00000507646.1:n.*854A>T
ENST00000683535.1:n.1569A>T
ENST00000684584.1:c.2602A>T	ENSP00000508044.1:p.Asn868Tyr
ENST00000684626.1:n.1685A>T
ENST00000684769.1:c.1629A>T	ENSP00000507691.1:n.1629A>T
ENST00000259008.7:c.3439A>T MANE Select	ENSP00000259008.2:p.Asn1147Tyr
ENST00000259008.6:c.3439A>T	ENSP00000259008.2:p.Asn1147Tyr
NM_032043.2:c.3439A>T , LRG_300t1:c.3439A>T	NP_114432.2:p.Asn1147Tyr
XM_011525332.1:c.3499A>T	XP_011523634.1:p.Asn1167Tyr
XM_011525333.1:c.3499A>T	XP_011523635.1:p.Asn1167Tyr
XM_011525334.1:c.3499A>T	XP_011523636.1:p.Asn1167Tyr
XM_011525335.1:c.3439A>T	XP_011523637.1:p.Asn1147Tyr
XM_011525336.1:c.3379A>T	XP_011523638.1:p.Asn1127Tyr
XM_011525337.1:c.3298A>T	XP_011523639.1:p.Asn1100Tyr
XM_011525338.1:c.3016A>T	XP_011523640.1:p.Asn1006Tyr
XM_011525332.3:c.3499A>T	XP_011523634.1:p.Asn1167Tyr
XM_011525333.3:c.3499A>T	XP_011523635.1:p.Asn1167Tyr
XM_011525334.2:c.3499A>T	XP_011523636.1:p.Asn1167Tyr
XM_011525335.3:c.3439A>T	XP_011523637.1:p.Asn1147Tyr
XM_011525336.2:c.3379A>T	XP_011523638.1:p.Asn1127Tyr
XM_011525337.2:c.3298A>T	XP_011523639.1:p.Asn1100Tyr
XM_011525338.2:c.3016A>T	XP_011523640.1:p.Asn1006Tyr
XM_017025200.1:c.2956A>T	XP_016880689.1:p.Asn986Tyr
XM_017025201.1:c.2956A>T	XP_016880690.1:p.Asn986Tyr
XM_017025202.1:c.1585A>T	XP_016880691.1:p.Asn529Tyr
XM_017025203.1:c.1585A>T	XP_016880692.1:p.Asn529Tyr
NM_032043.3:c.3439A>T MANE Select	NP_114432.2:p.Asn1147Tyr