Canonical Allele Identifier: CA15898186
Gene: BRIP1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4968451

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61849946A>C , CM000679.2:g.61849946A>C GRCh38
NC_000017.10:g.59927307A>C , CM000679.1:g.59927307A>C GRCh37
NC_000017.9:g.57282089A>C NCBI36
NG_007409.2:g.18614T>G , LRG_300:g.18614T>G

Transcript Alleles

HGVS Amino-acid change
NM_032043.2:c.380-690T>G , LRG_300t1:c.380-690T>G NP_114432.2:p.=
XM_011525332.1:c.380-690T>G XP_011523634.1:p.=
XM_011525333.1:c.380-690T>G XP_011523635.1:p.=
XM_011525334.1:c.380-690T>G XP_011523636.1:p.=
XM_011525335.1:c.380-690T>G XP_011523637.1:p.=
XM_011525336.1:c.380-690T>G XP_011523638.1:p.=
XM_011525337.1:c.380-690T>G XP_011523639.1:p.=
XM_011525338.1:c.25-2726T>G XP_011523640.1:p.=
XM_011525339.1:c.380-690T>G XP_011523641.1:p.=
XM_011525340.1:c.380-690T>G XP_011523642.1:p.=
XM_011525341.1:c.380-690T>G XP_011523643.1:p.=
XM_011525332.3:c.380-690T>G
XM_011525333.3:c.380-690T>G
XM_011525334.2:c.380-690T>G
XM_011525335.3:c.380-690T>G
XM_011525336.2:c.380-690T>G
XM_011525337.2:c.380-690T>G
XM_011525338.2:c.25-2726T>G
XM_011525339.3:c.380-690T>G
XM_011525340.3:c.380-690T>G
XM_011525341.3:c.380-690T>G
XM_017025200.1:c.25-2726T>G XP_016880689.1:p.=
ENST00000259008.6:c.380-690T>G ENSP00000259008.2:p.=
ENST00000577598.5:n.380-690T>G ENSP00000464654.1:p.=