Canonical Allele Identifier: CA3044590935

Gene: BRIP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685986_61685990delinsGGGTG , CM000679.2:g.61685986_61685990delinsGGGTG	GRCh38
NC_000017.10:g.59763347_59763351delinsGGGTG , CM000679.1:g.59763347_59763351delinsGGGTG	GRCh37
NC_000017.9:g.57118129_57118133delinsGGGTG	NCBI36
NG_007409.2:g.182570_182574delinsCACCC , LRG_300:g.182570_182574delinsCACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682066.1:c.2881_2885delinsCACCC	ENSP00000507191.1:n.2881_2885delinsCACCC
ENST00000682073.1:n.1491_1495delinsCACCC
ENST00000682433.1:n.1830_1834delinsCACCC
ENST00000682453.1:c.2751_2755delinsCACCC	ENSP00000506943.1:p.Ser919Pro
ENST00000682477.1:c.*2177_*2181delinsCACCC	ENSP00000507075.1:n.*2177_*2181delinsCACCC
ENST00000682589.1:n.8628_8632delinsCACCC
ENST00000682755.1:c.2529_2533delinsCACCC	ENSP00000507660.1:p.Ser845Pro
ENST00000682989.1:c.2610-1850_2610-1846delinsCACCC	ENSP00000507786.1:n.2610-1850_2610-1846delinsCACCC
ENST00000683039.1:c.2751_2755delinsCACCC	ENSP00000508303.1:p.Ser919Pro
ENST00000683235.1:c.*166_*170delinsCACCC	ENSP00000507646.1:n.*166_*170delinsCACCC
ENST00000683535.1:n.881_885delinsCACCC
ENST00000684471.1:n.1164_1168delinsCACCC
ENST00000684584.1:c.2069-1850_2069-1846delinsCACCC	ENSP00000508044.1:n.2069-1850_2069-1846delinsCACCC
ENST00000684626.1:n.997_1001delinsCACCC
ENST00000684769.1:c.941_945delinsCACCC	ENSP00000507691.1:n.941_945delinsCACCC
ENST00000259008.7:c.2751_2755delinsCACCC MANE Select	ENSP00000259008.2:p.Ser919Pro
ENST00000259008.6:c.2751_2755delinsCACCC	ENSP00000259008.2:p.Ser919Pro
ENST00000577598.5:c.2751_2755delinsCACCC	ENSP00000464654.1:p.Ser919Pro
NM_032043.2:c.2751_2755delinsCACCC , LRG_300t1:c.2751_2755delinsCACCC	NP_114432.2:p.Ser919Pro
XM_011525332.1:c.2811_2815delinsCACCC	XP_011523634.1:p.Ser939Pro
XM_011525333.1:c.2811_2815delinsCACCC	XP_011523635.1:p.Ser939Pro
XM_011525334.1:c.2811_2815delinsCACCC	XP_011523636.1:p.Ser939Pro
XM_011525335.1:c.2751_2755delinsCACCC	XP_011523637.1:p.Ser919Pro
XM_011525336.1:c.2691_2695delinsCACCC	XP_011523638.1:p.Ser899Pro
XM_011525337.1:c.2610_2614delinsCACCC	XP_011523639.1:p.Ser872Pro
XM_011525338.1:c.2328_2332delinsCACCC	XP_011523640.1:p.Ser778Pro
XM_011525332.3:c.2811_2815delinsCACCC	XP_011523634.1:p.Ser939Pro
XM_011525333.3:c.2811_2815delinsCACCC	XP_011523635.1:p.Ser939Pro
XM_011525334.2:c.2811_2815delinsCACCC	XP_011523636.1:p.Ser939Pro
XM_011525335.3:c.2751_2755delinsCACCC	XP_011523637.1:p.Ser919Pro
XM_011525336.2:c.2691_2695delinsCACCC	XP_011523638.1:p.Ser899Pro
XM_011525337.2:c.2610_2614delinsCACCC	XP_011523639.1:p.Ser872Pro
XM_011525338.2:c.2328_2332delinsCACCC	XP_011523640.1:p.Ser778Pro
XM_017025200.1:c.2268_2272delinsCACCC	XP_016880689.1:p.Ser758Pro
XM_017025201.1:c.2268_2272delinsCACCC	XP_016880690.1:p.Ser758Pro
XM_017025202.1:c.897_901delinsCACCC	XP_016880691.1:p.Ser301Pro
XM_017025203.1:c.897_901delinsCACCC	XP_016880692.1:p.Ser301Pro
NM_032043.3:c.2751_2755delinsCACCC MANE Select	NP_114432.2:p.Ser919Pro