Canonical Allele Identifier: CA501151080

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144676724
• MyVariant Identifiers: chr17:g.59820419A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61743058A>G , CM000679.2:g.61743058A>G	GRCh38
NC_000017.10:g.59820419A>G , CM000679.1:g.59820419A>G	GRCh37
NC_000017.9:g.57175201A>G	NCBI36
NG_007409.2:g.125502T>C , LRG_300:g.125502T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584322.2:c.2334T>C	ENSP00000463272.2:p.Ala778=
ENST00000682066.1:c.2464T>C	ENSP00000507191.1:n.2464T>C
ENST00000682073.1:n.1074T>C
ENST00000682433.1:n.1413T>C
ENST00000682453.1:c.2334T>C	ENSP00000506943.1:p.Ala778=
ENST00000682477.1:c.*1760T>C	ENSP00000507075.1:n.*1760T>C
ENST00000682589.1:n.8211T>C
ENST00000682755.1:c.2112T>C	ENSP00000507660.1:p.Ala704=
ENST00000682989.1:c.2334T>C	ENSP00000507786.1:p.Ala778=
ENST00000683039.1:c.2334T>C	ENSP00000508303.1:p.Ala778=
ENST00000683235.1:c.2334T>C	ENSP00000507646.1:p.Ala778=
ENST00000683381.1:c.2394T>C	ENSP00000508184.1:p.Ala798=
ENST00000683535.1:n.464T>C
ENST00000684471.1:n.747T>C
ENST00000684584.1:c.1827T>C	ENSP00000508044.1:p.Ala609=
ENST00000684769.1:c.399T>C	ENSP00000507691.1:p.Ala133=
ENST00000259008.7:c.2334T>C MANE Select	ENSP00000259008.2:p.Ala778=
ENST00000259008.6:c.2334T>C	ENSP00000259008.2:p.Ala778=
ENST00000577598.5:c.2334T>C	ENSP00000464654.1:p.Ala778=
ENST00000584322.1:c.317T>C
NM_032043.2:c.2334T>C , LRG_300t1:c.2334T>C	NP_114432.2:p.Ala778=
XM_011525332.1:c.2394T>C	XP_011523634.1:p.Ala798=
XM_011525333.1:c.2394T>C	XP_011523635.1:p.Ala798=
XM_011525334.1:c.2394T>C	XP_011523636.1:p.Ala798=
XM_011525335.1:c.2334T>C	XP_011523637.1:p.Ala778=
XM_011525336.1:c.2274T>C	XP_011523638.1:p.Ala758=
XM_011525337.1:c.2193T>C	XP_011523639.1:p.Ala731=
XM_011525338.1:c.1911T>C	XP_011523640.1:p.Ala637=
XM_011525339.1:c.2394T>C	XP_011523641.1:p.Ala798=
XM_011525340.1:c.2394T>C	XP_011523642.1:p.Ala798=
XR_934894.1:n.524-1123A>G
XM_011525332.3:c.2394T>C	XP_011523634.1:p.Ala798=
XM_011525333.3:c.2394T>C	XP_011523635.1:p.Ala798=
XM_011525334.2:c.2394T>C	XP_011523636.1:p.Ala798=
XM_011525335.3:c.2334T>C	XP_011523637.1:p.Ala778=
XM_011525336.2:c.2274T>C	XP_011523638.1:p.Ala758=
XM_011525337.2:c.2193T>C	XP_011523639.1:p.Ala731=
XM_011525338.2:c.1911T>C	XP_011523640.1:p.Ala637=
XM_011525339.3:c.2394T>C	XP_011523641.1:p.Ala798=
XM_011525340.3:c.2394T>C	XP_011523642.1:p.Ala798=
XM_017025200.1:c.1851T>C	XP_016880689.1:p.Ala617=
XM_017025201.1:c.1851T>C	XP_016880690.1:p.Ala617=
XM_017025202.1:c.480T>C	XP_016880691.1:p.Ala160=
XM_017025203.1:c.480T>C	XP_016880692.1:p.Ala160=
NM_032043.3:c.2334T>C MANE Select	NP_114432.2:p.Ala778=