Canonical Allele Identifier: CA2269154946
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61743021C= , CM000679.2:g.61743021C= GRCh38
NC_000017.10:g.59820382C= , CM000679.1:g.59820382C= GRCh37
NC_000017.9:g.57175164C= NCBI36
NG_007409.2:g.125539G= , LRG_300:g.125539G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584322.2:c.2371G= ENSP00000463272.2:p.Asp791=
ENST00000682066.1:c.2501G= ENSP00000507191.1:n.2501G=
ENST00000682073.1:n.1111G=
ENST00000682433.1:n.1450G=
ENST00000682453.1:c.2371G= ENSP00000506943.1:p.Asp791=
ENST00000682477.1:c.*1797G= ENSP00000507075.1:n.*1797G=
ENST00000682589.1:n.8248G=
ENST00000682755.1:c.2149G= ENSP00000507660.1:p.Asp717=
ENST00000682989.1:c.2371G= ENSP00000507786.1:p.Asp791=
ENST00000683039.1:c.2371G= ENSP00000508303.1:p.Asp791=
ENST00000683235.1:c.2371G= ENSP00000507646.1:p.Asp791=
ENST00000683381.1:c.2431G= ENSP00000508184.1:p.Asp811=
ENST00000683535.1:n.501G=
ENST00000684471.1:n.784G=
ENST00000684584.1:c.1864G= ENSP00000508044.1:p.Asp622=
ENST00000684769.1:c.436G= ENSP00000507691.1:p.Asp146=
ENST00000259008.7:c.2371G= MANE Select ENSP00000259008.2:p.Asp791=
ENST00000259008.6:c.2371G= ENSP00000259008.2:p.Asp791=
ENST00000577598.5:c.2371G= ENSP00000464654.1:p.Asp791=
ENST00000584322.1:c.354G=
NM_032043.2:c.2371G= , LRG_300t1:c.2371G= NP_114432.2:p.Asp791=
XM_011525332.1:c.2431G= XP_011523634.1:p.Asp811=
XM_011525333.1:c.2431G= XP_011523635.1:p.Asp811=
XM_011525334.1:c.2431G= XP_011523636.1:p.Asp811=
XM_011525335.1:c.2371G= XP_011523637.1:p.Asp791=
XM_011525336.1:c.2311G= XP_011523638.1:p.Asp771=
XM_011525337.1:c.2230G= XP_011523639.1:p.Asp744=
XM_011525338.1:c.1948G= XP_011523640.1:p.Asp650=
XM_011525339.1:c.2431G= XP_011523641.1:p.Asp811=
XM_011525340.1:c.2431G= XP_011523642.1:p.Asp811=
XR_934894.1:n.524-1160C=
XM_011525332.3:c.2431G= XP_011523634.1:p.Asp811=
XM_011525333.3:c.2431G= XP_011523635.1:p.Asp811=
XM_011525334.2:c.2431G= XP_011523636.1:p.Asp811=
XM_011525335.3:c.2371G= XP_011523637.1:p.Asp791=
XM_011525336.2:c.2311G= XP_011523638.1:p.Asp771=
XM_011525337.2:c.2230G= XP_011523639.1:p.Asp744=
XM_011525338.2:c.1948G= XP_011523640.1:p.Asp650=
XM_011525339.3:c.2431G= XP_011523641.1:p.Asp811=
XM_011525340.3:c.2431G= XP_011523642.1:p.Asp811=
XM_017025200.1:c.1888G= XP_016880689.1:p.Asp630=
XM_017025201.1:c.1888G= XP_016880690.1:p.Asp630=
XM_017025202.1:c.517G= XP_016880691.1:p.Asp173=
XM_017025203.1:c.517G= XP_016880692.1:p.Asp173=
NM_032043.3:c.2371G= MANE Select NP_114432.2:p.Asp791=