Canonical Allele Identifier: CA400479869

Gene: BRIP1

Linked Data

• dbSNP Id: rs587781744
• MyVariant Identifiers: chr17:g.59761336C>G (hg19) ; chr17:g.61683975C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683975C>G , CM000679.2:g.61683975C>G	GRCh38
NC_000017.10:g.59761336C>G , CM000679.1:g.59761336C>G	GRCh37
NC_000017.9:g.57116118C>G	NCBI36
NG_007409.2:g.184585G>C , LRG_300:g.184585G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682073.1:n.1811G>C
ENST00000682453.1:c.3071G>C	ENSP00000506943.1:p.Gly1024Ala
ENST00000682477.1:c.*2497G>C	ENSP00000507075.1:n.*2497G>C
ENST00000682589.1:n.8948G>C
ENST00000682755.1:c.2849G>C	ENSP00000507660.1:p.Gly950Ala
ENST00000682989.1:c.*162G>C	ENSP00000507786.1:n.*162G>C
ENST00000683039.1:c.3071G>C	ENSP00000508303.1:p.Gly1024Ala
ENST00000683235.1:c.*486G>C	ENSP00000507646.1:n.*486G>C
ENST00000683535.1:n.1201G>C
ENST00000684584.1:c.2234G>C	ENSP00000508044.1:p.Gly745Ala
ENST00000684626.1:n.1317G>C
ENST00000684769.1:c.1261G>C	ENSP00000507691.1:n.1261G>C
ENST00000259008.7:c.3071G>C MANE Select	ENSP00000259008.2:p.Gly1024Ala
ENST00000259008.6:c.3071G>C	ENSP00000259008.2:p.Gly1024Ala
NM_032043.2:c.3071G>C , LRG_300t1:c.3071G>C	NP_114432.2:p.Gly1024Ala
XM_011525332.1:c.3131G>C	XP_011523634.1:p.Gly1044Ala
XM_011525333.1:c.3131G>C	XP_011523635.1:p.Gly1044Ala
XM_011525334.1:c.3131G>C	XP_011523636.1:p.Gly1044Ala
XM_011525335.1:c.3071G>C	XP_011523637.1:p.Gly1024Ala
XM_011525336.1:c.3011G>C	XP_011523638.1:p.Gly1004Ala
XM_011525337.1:c.2930G>C	XP_011523639.1:p.Gly977Ala
XM_011525338.1:c.2648G>C	XP_011523640.1:p.Gly883Ala
XM_011525332.3:c.3131G>C	XP_011523634.1:p.Gly1044Ala
XM_011525333.3:c.3131G>C	XP_011523635.1:p.Gly1044Ala
XM_011525334.2:c.3131G>C	XP_011523636.1:p.Gly1044Ala
XM_011525335.3:c.3071G>C	XP_011523637.1:p.Gly1024Ala
XM_011525336.2:c.3011G>C	XP_011523638.1:p.Gly1004Ala
XM_011525337.2:c.2930G>C	XP_011523639.1:p.Gly977Ala
XM_011525338.2:c.2648G>C	XP_011523640.1:p.Gly883Ala
XM_017025200.1:c.2588G>C	XP_016880689.1:p.Gly863Ala
XM_017025201.1:c.2588G>C	XP_016880690.1:p.Gly863Ala
XM_017025202.1:c.1217G>C	XP_016880691.1:p.Gly406Ala
XM_017025203.1:c.1217G>C	XP_016880692.1:p.Gly406Ala
NM_032043.3:c.3071G>C MANE Select	NP_114432.2:p.Gly1024Ala