Canonical Allele Identifier: CA16615470

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 407862
• ClinVar RCV Id: RCV000466152 ; RCV003153616
• dbSNP Id: rs1060501773
• gnomAD v4: 17-61683693-T-C
• MyVariant Identifiers: chr17:g.59761054T>C (hg19) ; chr17:g.61683693T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683693T>C , CM000679.2:g.61683693T>C	GRCh38
NC_000017.10:g.59761054T>C , CM000679.1:g.59761054T>C	GRCh37
NC_000017.9:g.57115836T>C	NCBI36
NG_007409.2:g.184867A>G , LRG_300:g.184867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2093A>G
ENST00000682453.1:c.3353A>G	ENSP00000506943.1:p.Asn1118Ser
ENST00000682477.1:c.*2779A>G	ENSP00000507075.1:n.*2779A>G
ENST00000682589.1:n.9230A>G
ENST00000682755.1:c.3131A>G	ENSP00000507660.1:p.Asn1044Ser
ENST00000682989.1:c.*444A>G	ENSP00000507786.1:n.*444A>G
ENST00000683039.1:c.3353A>G	ENSP00000508303.1:p.Asn1118Ser
ENST00000683235.1:c.*768A>G	ENSP00000507646.1:n.*768A>G
ENST00000683535.1:n.1483A>G
ENST00000684584.1:c.2516A>G	ENSP00000508044.1:p.Asn839Ser
ENST00000684626.1:n.1599A>G
ENST00000684769.1:c.1543A>G	ENSP00000507691.1:n.1543A>G
ENST00000259008.7:c.3353A>G MANE Select	ENSP00000259008.2:p.Asn1118Ser
ENST00000259008.6:c.3353A>G	ENSP00000259008.2:p.Asn1118Ser
NM_032043.2:c.3353A>G , LRG_300t1:c.3353A>G	NP_114432.2:p.Asn1118Ser
XM_011525332.1:c.3413A>G	XP_011523634.1:p.Asn1138Ser
XM_011525333.1:c.3413A>G	XP_011523635.1:p.Asn1138Ser
XM_011525334.1:c.3413A>G	XP_011523636.1:p.Asn1138Ser
XM_011525335.1:c.3353A>G	XP_011523637.1:p.Asn1118Ser
XM_011525336.1:c.3293A>G	XP_011523638.1:p.Asn1098Ser
XM_011525337.1:c.3212A>G	XP_011523639.1:p.Asn1071Ser
XM_011525338.1:c.2930A>G	XP_011523640.1:p.Asn977Ser
XM_011525332.3:c.3413A>G	XP_011523634.1:p.Asn1138Ser
XM_011525333.3:c.3413A>G	XP_011523635.1:p.Asn1138Ser
XM_011525334.2:c.3413A>G	XP_011523636.1:p.Asn1138Ser
XM_011525335.3:c.3353A>G	XP_011523637.1:p.Asn1118Ser
XM_011525336.2:c.3293A>G	XP_011523638.1:p.Asn1098Ser
XM_011525337.2:c.3212A>G	XP_011523639.1:p.Asn1071Ser
XM_011525338.2:c.2930A>G	XP_011523640.1:p.Asn977Ser
XM_017025200.1:c.2870A>G	XP_016880689.1:p.Asn957Ser
XM_017025201.1:c.2870A>G	XP_016880690.1:p.Asn957Ser
XM_017025202.1:c.1499A>G	XP_016880691.1:p.Asn500Ser
XM_017025203.1:c.1499A>G	XP_016880692.1:p.Asn500Ser
NM_032043.3:c.3353A>G MANE Select	NP_114432.2:p.Asn1118Ser