Canonical Allele Identifier: CA400478839

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 2692012
• ClinVar RCV Id: RCV003494209
• dbSNP Id: rs1603275152
• MyVariant Identifiers: chr17:g.59761021G>A (hg19) ; chr17:g.61683660G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683660G>A , CM000679.2:g.61683660G>A	GRCh38
NC_000017.10:g.59761021G>A , CM000679.1:g.59761021G>A	GRCh37
NC_000017.9:g.57115803G>A	NCBI36
NG_007409.2:g.184900C>T , LRG_300:g.184900C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2126C>T
ENST00000682453.1:c.3386C>T	ENSP00000506943.1:p.Ser1129Phe
ENST00000682477.1:c.*2812C>T	ENSP00000507075.1:n.*2812C>T
ENST00000682589.1:n.9263C>T
ENST00000682755.1:c.3164C>T	ENSP00000507660.1:p.Ser1055Phe
ENST00000682989.1:c.*477C>T	ENSP00000507786.1:n.*477C>T
ENST00000683039.1:c.3386C>T	ENSP00000508303.1:p.Ser1129Phe
ENST00000683235.1:c.*801C>T	ENSP00000507646.1:n.*801C>T
ENST00000683535.1:n.1516C>T
ENST00000684584.1:c.2549C>T	ENSP00000508044.1:p.Ser850Phe
ENST00000684626.1:n.1632C>T
ENST00000684769.1:c.1576C>T	ENSP00000507691.1:n.1576C>T
ENST00000259008.7:c.3386C>T MANE Select	ENSP00000259008.2:p.Ser1129Phe
ENST00000259008.6:c.3386C>T	ENSP00000259008.2:p.Ser1129Phe
NM_032043.2:c.3386C>T , LRG_300t1:c.3386C>T	NP_114432.2:p.Ser1129Phe
XM_011525332.1:c.3446C>T	XP_011523634.1:p.Ser1149Phe
XM_011525333.1:c.3446C>T	XP_011523635.1:p.Ser1149Phe
XM_011525334.1:c.3446C>T	XP_011523636.1:p.Ser1149Phe
XM_011525335.1:c.3386C>T	XP_011523637.1:p.Ser1129Phe
XM_011525336.1:c.3326C>T	XP_011523638.1:p.Ser1109Phe
XM_011525337.1:c.3245C>T	XP_011523639.1:p.Ser1082Phe
XM_011525338.1:c.2963C>T	XP_011523640.1:p.Ser988Phe
XM_011525332.3:c.3446C>T	XP_011523634.1:p.Ser1149Phe
XM_011525333.3:c.3446C>T	XP_011523635.1:p.Ser1149Phe
XM_011525334.2:c.3446C>T	XP_011523636.1:p.Ser1149Phe
XM_011525335.3:c.3386C>T	XP_011523637.1:p.Ser1129Phe
XM_011525336.2:c.3326C>T	XP_011523638.1:p.Ser1109Phe
XM_011525337.2:c.3245C>T	XP_011523639.1:p.Ser1082Phe
XM_011525338.2:c.2963C>T	XP_011523640.1:p.Ser988Phe
XM_017025200.1:c.2903C>T	XP_016880689.1:p.Ser968Phe
XM_017025201.1:c.2903C>T	XP_016880690.1:p.Ser968Phe
XM_017025202.1:c.1532C>T	XP_016880691.1:p.Ser511Phe
XM_017025203.1:c.1532C>T	XP_016880692.1:p.Ser511Phe
NM_032043.3:c.3386C>T MANE Select	NP_114432.2:p.Ser1129Phe