Canonical Allele Identifier: CA292282217

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61863291G>A , CM000679.2:g.61863291G>A	GRCh38
NC_000017.10:g.59940652G>A , CM000679.1:g.59940652G>A	GRCh37
NC_000017.9:g.57295434G>A	NCBI36
NG_007409.2:g.5269C>T , LRG_300:g.5269C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032043.3:c.-38C>T MANE Select	NP_114432.2:n.-38C>T
ENST00000259008.7:c.-38C>T MANE Select	ENSP00000259008.2:n.-38C>T
NM_032043.2:c.-38C>T , LRG_300t1:c.-38C>T	NP_114432.2:n.-38C>T
ENST00000259008.6:c.-38C>T	ENSP00000259008.2:n.-38C>T
ENST00000577913.1:c.-204C>T	ENSP00000462274.1:n.-204C>T
ENST00000577913.2:c.-34C>T	ENSP00000462274.2:n.-34C>T
ENST00000584322.2:c.-38C>T	ENSP00000463272.2:n.-38C>T
ENST00000682369.1:c.-38C>T	ENSP00000507450.1:n.-38C>T
ENST00000682453.1:c.-38C>T	ENSP00000506943.1:n.-38C>T
ENST00000682477.1:c.-38C>T	ENSP00000507075.1:n.-38C>T
ENST00000682989.1:c.-34C>T	ENSP00000507786.1:n.-34C>T
ENST00000683039.1:c.-204C>T	ENSP00000508303.1:n.-204C>T
ENST00000683235.1:c.-34C>T	ENSP00000507646.1:n.-34C>T
ENST00000683381.1:c.-38C>T	ENSP00000508184.1:n.-38C>T
ENST00000683672.1:c.-100C>T	ENSP00000506781.1:n.-100C>T
XM_011525332.1:c.-38C>T	XP_011523634.1:n.-38C>T
XM_011525332.3:c.-38C>T	XP_011523634.1:n.-38C>T
XM_011525333.1:c.-34C>T	XP_011523635.1:n.-34C>T
XM_011525333.3:c.-34C>T	XP_011523635.1:n.-34C>T
XM_011525335.1:c.-38C>T	XP_011523637.1:n.-38C>T
XM_011525335.3:c.-38C>T	XP_011523637.1:n.-38C>T
XM_011525336.1:c.-38C>T	XP_011523638.1:n.-38C>T
XM_011525336.2:c.-38C>T	XP_011523638.1:n.-38C>T
XM_011525337.1:c.-38C>T	XP_011523639.1:n.-38C>T
XM_011525337.2:c.-38C>T	XP_011523639.1:n.-38C>T
XM_011525339.1:c.-38C>T	XP_011523641.1:n.-38C>T
XM_011525339.3:c.-38C>T	XP_011523641.1:n.-38C>T
XM_011525340.1:c.-38C>T	XP_011523642.1:n.-38C>T
XM_011525340.3:c.-38C>T	XP_011523642.1:n.-38C>T
XM_011525341.1:c.-38C>T	XP_011523643.1:n.-38C>T
XM_011525341.3:c.-38C>T	XP_011523643.1:n.-38C>T