Canonical Allele Identifier: CA14438103
Gene: BRIP1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2191249

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61758503T>G , CM000679.2:g.61758503T>G GRCh38
NC_000017.10:g.59835864T>G , CM000679.1:g.59835864T>G GRCh37
NC_000017.9:g.57190646T>G NCBI36
NG_007409.2:g.110057A>C , LRG_300:g.110057A>C

Transcript Alleles

HGVS Amino-acid change
NM_032043.2:c.2098-13912A>C , LRG_300t1:c.2098-13912A>C NP_114432.2:p.=
XM_011525332.1:c.2158-13912A>C XP_011523634.1:p.=
XM_011525333.1:c.2158-13912A>C XP_011523635.1:p.=
XM_011525334.1:c.2158-13912A>C XP_011523636.1:p.=
XM_011525335.1:c.2098-13912A>C XP_011523637.1:p.=
XM_011525336.1:c.2038-13912A>C XP_011523638.1:p.=
XM_011525337.1:c.1957-13912A>C XP_011523639.1:p.=
XM_011525338.1:c.1675-13912A>C XP_011523640.1:p.=
XM_011525339.1:c.2158-13912A>C XP_011523641.1:p.=
XM_011525340.1:c.2158-13912A>C XP_011523642.1:p.=
XM_011525332.3:c.2158-13912A>C XP_011523634.1:p.=
XM_011525333.3:c.2158-13912A>C XP_011523635.1:p.=
XM_011525334.2:c.2158-13912A>C XP_011523636.1:p.=
XM_011525335.3:c.2098-13912A>C XP_011523637.1:p.=
XM_011525336.2:c.2038-13912A>C XP_011523638.1:p.=
XM_011525337.2:c.1957-13912A>C XP_011523639.1:p.=
XM_011525338.2:c.1675-13912A>C XP_011523640.1:p.=
XM_011525339.3:c.2158-13912A>C XP_011523641.1:p.=
XM_011525340.3:c.2158-13912A>C XP_011523642.1:p.=
XM_017025200.1:c.1615-13912A>C XP_016880689.1:p.=
XM_017025201.1:c.1615-13912A>C XP_016880690.1:p.=
XM_017025202.1:c.244-13912A>C XP_016880691.1:p.=
XM_017025203.1:c.244-13912A>C XP_016880692.1:p.=
ENST00000259008.6:c.2098-13912A>C ENSP00000259008.2:p.=
ENST00000577598.5:n.2098-13912A>C ENSP00000464654.1:p.=
ENST00000584322.1:n.81-13912A>C