Canonical Allele Identifier: CA501335572

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144109441
• MyVariant Identifiers: chr17:g.59763264T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685903T>A , CM000679.2:g.61685903T>A	GRCh38
NC_000017.10:g.59763264T>A , CM000679.1:g.59763264T>A	GRCh37
NC_000017.9:g.57118046T>A	NCBI36
NG_007409.2:g.182657A>T , LRG_300:g.182657A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682066.1:c.2968A>T	ENSP00000507191.1:n.2968A>T
ENST00000682073.1:n.1578A>T
ENST00000682433.1:n.1917A>T
ENST00000682453.1:c.2838A>T	ENSP00000506943.1:p.Leu946=
ENST00000682477.1:c.*2264A>T	ENSP00000507075.1:n.*2264A>T
ENST00000682589.1:n.8715A>T
ENST00000682755.1:c.2616A>T	ENSP00000507660.1:p.Leu872=
ENST00000682989.1:c.2610-1763A>T	ENSP00000507786.1:n.2610-1763A>T
ENST00000683039.1:c.2838A>T	ENSP00000508303.1:p.Leu946=
ENST00000683235.1:c.*253A>T	ENSP00000507646.1:n.*253A>T
ENST00000683535.1:n.968A>T
ENST00000684471.1:n.1251A>T
ENST00000684584.1:c.2069-1763A>T	ENSP00000508044.1:n.2069-1763A>T
ENST00000684626.1:n.1084A>T
ENST00000684769.1:c.1028A>T	ENSP00000507691.1:n.1028A>T
ENST00000259008.7:c.2838A>T MANE Select	ENSP00000259008.2:p.Leu946=
ENST00000259008.6:c.2838A>T	ENSP00000259008.2:p.Leu946=
ENST00000577598.5:c.2838A>T	ENSP00000464654.1:p.Leu946=
NM_032043.2:c.2838A>T , LRG_300t1:c.2838A>T	NP_114432.2:p.Leu946=
XM_011525332.1:c.2898A>T	XP_011523634.1:p.Leu966=
XM_011525333.1:c.2898A>T	XP_011523635.1:p.Leu966=
XM_011525334.1:c.2898A>T	XP_011523636.1:p.Leu966=
XM_011525335.1:c.2838A>T	XP_011523637.1:p.Leu946=
XM_011525336.1:c.2778A>T	XP_011523638.1:p.Leu926=
XM_011525337.1:c.2697A>T	XP_011523639.1:p.Leu899=
XM_011525338.1:c.2415A>T	XP_011523640.1:p.Leu805=
XM_011525332.3:c.2898A>T	XP_011523634.1:p.Leu966=
XM_011525333.3:c.2898A>T	XP_011523635.1:p.Leu966=
XM_011525334.2:c.2898A>T	XP_011523636.1:p.Leu966=
XM_011525335.3:c.2838A>T	XP_011523637.1:p.Leu946=
XM_011525336.2:c.2778A>T	XP_011523638.1:p.Leu926=
XM_011525337.2:c.2697A>T	XP_011523639.1:p.Leu899=
XM_011525338.2:c.2415A>T	XP_011523640.1:p.Leu805=
XM_017025200.1:c.2355A>T	XP_016880689.1:p.Leu785=
XM_017025201.1:c.2355A>T	XP_016880690.1:p.Leu785=
XM_017025202.1:c.984A>T	XP_016880691.1:p.Leu328=
XM_017025203.1:c.984A>T	XP_016880692.1:p.Leu328=
NM_032043.3:c.2838A>T MANE Select	NP_114432.2:p.Leu946=