Canonical Allele Identifier: CA400481325

Gene: BRIP1

Linked Data

• dbSNP Id: rs1603276576
• MyVariant Identifiers: chr17:g.59763252T>A (hg19) ; chr17:g.61685891T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685891T>A , CM000679.2:g.61685891T>A	GRCh38
NC_000017.10:g.59763252T>A , CM000679.1:g.59763252T>A	GRCh37
NC_000017.9:g.57118034T>A	NCBI36
NG_007409.2:g.182669A>T , LRG_300:g.182669A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2980A>T	ENSP00000507191.1:n.2980A>T
ENST00000682073.1:n.1590A>T
ENST00000682433.1:n.1929A>T
ENST00000682453.1:c.2850A>T	ENSP00000506943.1:p.Lys950Asn
ENST00000682477.1:c.*2276A>T	ENSP00000507075.1:n.*2276A>T
ENST00000682589.1:n.8727A>T
ENST00000682755.1:c.2628A>T	ENSP00000507660.1:p.Lys876Asn
ENST00000682989.1:c.2610-1751A>T	ENSP00000507786.1:n.2610-1751A>T
ENST00000683039.1:c.2850A>T	ENSP00000508303.1:p.Lys950Asn
ENST00000683235.1:c.*265A>T	ENSP00000507646.1:n.*265A>T
ENST00000683535.1:n.980A>T
ENST00000684471.1:n.1263A>T
ENST00000684584.1:c.2069-1751A>T	ENSP00000508044.1:n.2069-1751A>T
ENST00000684626.1:n.1096A>T
ENST00000684769.1:c.1040A>T	ENSP00000507691.1:n.1040A>T
ENST00000259008.7:c.2850A>T MANE Select	ENSP00000259008.2:p.Lys950Asn
ENST00000259008.6:c.2850A>T	ENSP00000259008.2:p.Lys950Asn
ENST00000577598.5:c.2850A>T	ENSP00000464654.1:p.Lys950Asn
NM_032043.2:c.2850A>T , LRG_300t1:c.2850A>T	NP_114432.2:p.Lys950Asn
XM_011525332.1:c.2910A>T	XP_011523634.1:p.Lys970Asn
XM_011525333.1:c.2910A>T	XP_011523635.1:p.Lys970Asn
XM_011525334.1:c.2910A>T	XP_011523636.1:p.Lys970Asn
XM_011525335.1:c.2850A>T	XP_011523637.1:p.Lys950Asn
XM_011525336.1:c.2790A>T	XP_011523638.1:p.Lys930Asn
XM_011525337.1:c.2709A>T	XP_011523639.1:p.Lys903Asn
XM_011525338.1:c.2427A>T	XP_011523640.1:p.Lys809Asn
XM_011525332.3:c.2910A>T	XP_011523634.1:p.Lys970Asn
XM_011525333.3:c.2910A>T	XP_011523635.1:p.Lys970Asn
XM_011525334.2:c.2910A>T	XP_011523636.1:p.Lys970Asn
XM_011525335.3:c.2850A>T	XP_011523637.1:p.Lys950Asn
XM_011525336.2:c.2790A>T	XP_011523638.1:p.Lys930Asn
XM_011525337.2:c.2709A>T	XP_011523639.1:p.Lys903Asn
XM_011525338.2:c.2427A>T	XP_011523640.1:p.Lys809Asn
XM_017025200.1:c.2367A>T	XP_016880689.1:p.Lys789Asn
XM_017025201.1:c.2367A>T	XP_016880690.1:p.Lys789Asn
XM_017025202.1:c.996A>T	XP_016880691.1:p.Lys332Asn
XM_017025203.1:c.996A>T	XP_016880692.1:p.Lys332Asn
NM_032043.3:c.2850A>T MANE Select	NP_114432.2:p.Lys950Asn