Canonical Allele Identifier: CA400477929

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59760769A>C (hg19) ; chr17:g.61683408A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683408A>C , CM000679.2:g.61683408A>C	GRCh38
NC_000017.10:g.59760769A>C , CM000679.1:g.59760769A>C	GRCh37
NC_000017.9:g.57115551A>C	NCBI36
NG_007409.2:g.185152T>G , LRG_300:g.185152T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2378T>G
ENST00000682453.1:c.3638T>G	ENSP00000506943.1:p.Val1213Gly
ENST00000682477.1:c.*3064T>G	ENSP00000507075.1:n.*3064T>G
ENST00000682589.1:n.9515T>G
ENST00000682755.1:c.3416T>G	ENSP00000507660.1:p.Val1139Gly
ENST00000682989.1:c.*729T>G	ENSP00000507786.1:n.*729T>G
ENST00000683039.1:c.3638T>G	ENSP00000508303.1:p.Val1213Gly
ENST00000683235.1:c.*1053T>G	ENSP00000507646.1:n.*1053T>G
ENST00000683535.1:n.1768T>G
ENST00000684584.1:c.2801T>G	ENSP00000508044.1:p.Val934Gly
ENST00000684626.1:n.1884T>G
ENST00000684769.1:c.1828T>G	ENSP00000507691.1:n.1828T>G
ENST00000259008.7:c.3638T>G MANE Select	ENSP00000259008.2:p.Val1213Gly
ENST00000259008.6:c.3638T>G	ENSP00000259008.2:p.Val1213Gly
NM_032043.2:c.3638T>G , LRG_300t1:c.3638T>G	NP_114432.2:p.Val1213Gly
XM_011525332.1:c.3698T>G	XP_011523634.1:p.Val1233Gly
XM_011525333.1:c.3698T>G	XP_011523635.1:p.Val1233Gly
XM_011525334.1:c.3698T>G	XP_011523636.1:p.Val1233Gly
XM_011525335.1:c.3638T>G	XP_011523637.1:p.Val1213Gly
XM_011525336.1:c.3578T>G	XP_011523638.1:p.Val1193Gly
XM_011525337.1:c.3497T>G	XP_011523639.1:p.Val1166Gly
XM_011525338.1:c.3215T>G	XP_011523640.1:p.Val1072Gly
XM_011525332.3:c.3698T>G	XP_011523634.1:p.Val1233Gly
XM_011525333.3:c.3698T>G	XP_011523635.1:p.Val1233Gly
XM_011525334.2:c.3698T>G	XP_011523636.1:p.Val1233Gly
XM_011525335.3:c.3638T>G	XP_011523637.1:p.Val1213Gly
XM_011525336.2:c.3578T>G	XP_011523638.1:p.Val1193Gly
XM_011525337.2:c.3497T>G	XP_011523639.1:p.Val1166Gly
XM_011525338.2:c.3215T>G	XP_011523640.1:p.Val1072Gly
XM_017025200.1:c.3155T>G	XP_016880689.1:p.Val1052Gly
XM_017025201.1:c.3155T>G	XP_016880690.1:p.Val1052Gly
XM_017025202.1:c.1784T>G	XP_016880691.1:p.Val595Gly
XM_017025203.1:c.1784T>G	XP_016880692.1:p.Val595Gly
NM_032043.3:c.3638T>G MANE Select	NP_114432.2:p.Val1213Gly