Canonical Allele Identifier: CA10583610

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 241659
• ClinVar RCV Id: RCV000233279
• dbSNP Id: rs878855156
• MyVariant Identifiers: chr17:g.59760707A>G (hg19) ; chr17:g.61683346A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683346A>G , CM000679.2:g.61683346A>G	GRCh38
NC_000017.10:g.59760707A>G , CM000679.1:g.59760707A>G	GRCh37
NC_000017.9:g.57115489A>G	NCBI36
NG_007409.2:g.185214T>C , LRG_300:g.185214T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2440T>C
ENST00000682453.1:c.3700T>C	ENSP00000506943.1:p.Phe1234Leu
ENST00000682477.1:c.*3126T>C	ENSP00000507075.1:n.*3126T>C
ENST00000682589.1:n.9577T>C
ENST00000682755.1:c.3478T>C	ENSP00000507660.1:p.Phe1160Leu
ENST00000682989.1:c.*791T>C	ENSP00000507786.1:n.*791T>C
ENST00000683039.1:c.3700T>C	ENSP00000508303.1:p.Phe1234Leu
ENST00000683235.1:c.*1115T>C	ENSP00000507646.1:n.*1115T>C
ENST00000683535.1:n.1830T>C
ENST00000684584.1:c.2863T>C	ENSP00000508044.1:p.Phe955Leu
ENST00000684626.1:n.1946T>C
ENST00000684769.1:c.1890T>C	ENSP00000507691.1:n.1890T>C
ENST00000259008.7:c.3700T>C MANE Select	ENSP00000259008.2:p.Phe1234Leu
ENST00000259008.6:c.3700T>C	ENSP00000259008.2:p.Phe1234Leu
NM_032043.2:c.3700T>C , LRG_300t1:c.3700T>C	NP_114432.2:p.Phe1234Leu
XM_011525332.1:c.3760T>C	XP_011523634.1:p.Phe1254Leu
XM_011525333.1:c.3760T>C	XP_011523635.1:p.Phe1254Leu
XM_011525334.1:c.3760T>C	XP_011523636.1:p.Phe1254Leu
XM_011525335.1:c.3700T>C	XP_011523637.1:p.Phe1234Leu
XM_011525336.1:c.3640T>C	XP_011523638.1:p.Phe1214Leu
XM_011525337.1:c.3559T>C	XP_011523639.1:p.Phe1187Leu
XM_011525338.1:c.3277T>C	XP_011523640.1:p.Phe1093Leu
XM_011525332.3:c.3760T>C	XP_011523634.1:p.Phe1254Leu
XM_011525333.3:c.3760T>C	XP_011523635.1:p.Phe1254Leu
XM_011525334.2:c.3760T>C	XP_011523636.1:p.Phe1254Leu
XM_011525335.3:c.3700T>C	XP_011523637.1:p.Phe1234Leu
XM_011525336.2:c.3640T>C	XP_011523638.1:p.Phe1214Leu
XM_011525337.2:c.3559T>C	XP_011523639.1:p.Phe1187Leu
XM_011525338.2:c.3277T>C	XP_011523640.1:p.Phe1093Leu
XM_017025200.1:c.3217T>C	XP_016880689.1:p.Phe1073Leu
XM_017025201.1:c.3217T>C	XP_016880690.1:p.Phe1073Leu
XM_017025202.1:c.1846T>C	XP_016880691.1:p.Phe616Leu
XM_017025203.1:c.1846T>C	XP_016880692.1:p.Phe616Leu
NM_032043.3:c.3700T>C MANE Select	NP_114432.2:p.Phe1234Leu