Canonical Allele Identifier: CA400478833

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144077816
• MyVariant Identifiers: chr17:g.59761016A>T (hg19) ; chr17:g.61683655A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683655A>T , CM000679.2:g.61683655A>T	GRCh38
NC_000017.10:g.59761016A>T , CM000679.1:g.59761016A>T	GRCh37
NC_000017.9:g.57115798A>T	NCBI36
NG_007409.2:g.184905T>A , LRG_300:g.184905T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2131T>A
ENST00000682453.1:c.3391T>A	ENSP00000506943.1:p.Tyr1131Asn
ENST00000682477.1:c.*2817T>A	ENSP00000507075.1:n.*2817T>A
ENST00000682589.1:n.9268T>A
ENST00000682755.1:c.3169T>A	ENSP00000507660.1:p.Tyr1057Asn
ENST00000682989.1:c.*482T>A	ENSP00000507786.1:n.*482T>A
ENST00000683039.1:c.3391T>A	ENSP00000508303.1:p.Tyr1131Asn
ENST00000683235.1:c.*806T>A	ENSP00000507646.1:n.*806T>A
ENST00000683535.1:n.1521T>A
ENST00000684584.1:c.2554T>A	ENSP00000508044.1:p.Tyr852Asn
ENST00000684626.1:n.1637T>A
ENST00000684769.1:c.1581T>A	ENSP00000507691.1:n.1581T>A
ENST00000259008.7:c.3391T>A MANE Select	ENSP00000259008.2:p.Tyr1131Asn
ENST00000259008.6:c.3391T>A	ENSP00000259008.2:p.Tyr1131Asn
NM_032043.2:c.3391T>A , LRG_300t1:c.3391T>A	NP_114432.2:p.Tyr1131Asn
XM_011525332.1:c.3451T>A	XP_011523634.1:p.Tyr1151Asn
XM_011525333.1:c.3451T>A	XP_011523635.1:p.Tyr1151Asn
XM_011525334.1:c.3451T>A	XP_011523636.1:p.Tyr1151Asn
XM_011525335.1:c.3391T>A	XP_011523637.1:p.Tyr1131Asn
XM_011525336.1:c.3331T>A	XP_011523638.1:p.Tyr1111Asn
XM_011525337.1:c.3250T>A	XP_011523639.1:p.Tyr1084Asn
XM_011525338.1:c.2968T>A	XP_011523640.1:p.Tyr990Asn
XM_011525332.3:c.3451T>A	XP_011523634.1:p.Tyr1151Asn
XM_011525333.3:c.3451T>A	XP_011523635.1:p.Tyr1151Asn
XM_011525334.2:c.3451T>A	XP_011523636.1:p.Tyr1151Asn
XM_011525335.3:c.3391T>A	XP_011523637.1:p.Tyr1131Asn
XM_011525336.2:c.3331T>A	XP_011523638.1:p.Tyr1111Asn
XM_011525337.2:c.3250T>A	XP_011523639.1:p.Tyr1084Asn
XM_011525338.2:c.2968T>A	XP_011523640.1:p.Tyr990Asn
XM_017025200.1:c.2908T>A	XP_016880689.1:p.Tyr970Asn
XM_017025201.1:c.2908T>A	XP_016880690.1:p.Tyr970Asn
XM_017025202.1:c.1537T>A	XP_016880691.1:p.Tyr513Asn
XM_017025203.1:c.1537T>A	XP_016880692.1:p.Tyr513Asn
NM_032043.3:c.3391T>A MANE Select	NP_114432.2:p.Tyr1131Asn