Canonical Allele Identifier: CA501335547

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59761389A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61684028A>G , CM000679.2:g.61684028A>G	GRCh38
NC_000017.10:g.59761389A>G , CM000679.1:g.59761389A>G	GRCh37
NC_000017.9:g.57116171A>G	NCBI36
NG_007409.2:g.184532T>C , LRG_300:g.184532T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1758T>C
ENST00000682453.1:c.3018T>C	ENSP00000506943.1:p.Asn1006=
ENST00000682477.1:c.*2444T>C	ENSP00000507075.1:n.*2444T>C
ENST00000682589.1:n.8895T>C
ENST00000682755.1:c.2796T>C	ENSP00000507660.1:p.Asn932=
ENST00000682989.1:c.*109T>C	ENSP00000507786.1:n.*109T>C
ENST00000683039.1:c.3018T>C	ENSP00000508303.1:p.Asn1006=
ENST00000683235.1:c.*433T>C	ENSP00000507646.1:n.*433T>C
ENST00000683535.1:n.1148T>C
ENST00000684584.1:c.2181T>C	ENSP00000508044.1:p.Asn727=
ENST00000684626.1:n.1264T>C
ENST00000684769.1:c.1208T>C	ENSP00000507691.1:n.1208T>C
ENST00000259008.7:c.3018T>C MANE Select	ENSP00000259008.2:p.Asn1006=
ENST00000259008.6:c.3018T>C	ENSP00000259008.2:p.Asn1006=
NM_032043.2:c.3018T>C , LRG_300t1:c.3018T>C	NP_114432.2:p.Asn1006=
XM_011525332.1:c.3078T>C	XP_011523634.1:p.Asn1026=
XM_011525333.1:c.3078T>C	XP_011523635.1:p.Asn1026=
XM_011525334.1:c.3078T>C	XP_011523636.1:p.Asn1026=
XM_011525335.1:c.3018T>C	XP_011523637.1:p.Asn1006=
XM_011525336.1:c.2958T>C	XP_011523638.1:p.Asn986=
XM_011525337.1:c.2877T>C	XP_011523639.1:p.Asn959=
XM_011525338.1:c.2595T>C	XP_011523640.1:p.Asn865=
XM_011525332.3:c.3078T>C	XP_011523634.1:p.Asn1026=
XM_011525333.3:c.3078T>C	XP_011523635.1:p.Asn1026=
XM_011525334.2:c.3078T>C	XP_011523636.1:p.Asn1026=
XM_011525335.3:c.3018T>C	XP_011523637.1:p.Asn1006=
XM_011525336.2:c.2958T>C	XP_011523638.1:p.Asn986=
XM_011525337.2:c.2877T>C	XP_011523639.1:p.Asn959=
XM_011525338.2:c.2595T>C	XP_011523640.1:p.Asn865=
XM_017025200.1:c.2535T>C	XP_016880689.1:p.Asn845=
XM_017025201.1:c.2535T>C	XP_016880690.1:p.Asn845=
XM_017025202.1:c.1164T>C	XP_016880691.1:p.Asn388=
XM_017025203.1:c.1164T>C	XP_016880692.1:p.Asn388=
NM_032043.3:c.3018T>C MANE Select	NP_114432.2:p.Asn1006=