Canonical Allele Identifier: CA2260783302

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092673_43092675delinsCAA , CM000679.2:g.43092673_43092675delinsCAA	GRCh38
NC_000017.10:g.41244690_41244692delinsCAA , CM000679.1:g.41244690_41244692delinsCAA	GRCh37
NC_000017.9:g.38498216_38498218delinsCAA	NCBI36
NG_005905.2:g.125309_125311delinsTTG , LRG_292:g.125309_125311delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.2920_2922delinsTTG
ENST00000461574.2:c.2856_2858delinsTTG	ENSP00000417241.2:p.Phe952=
ENST00000470026.6:c.2856_2858delinsTTG	ENSP00000419274.2:p.Phe952=
ENST00000473961.6:c.2730_2732delinsTTG	ENSP00000420201.2:p.Phe910=
ENST00000476777.6:c.2853_2855delinsTTG	ENSP00000417554.2:p.Phe951=
ENST00000477152.6:c.2778_2780delinsTTG	ENSP00000419988.2:p.Phe926=
ENST00000478531.6:c.785-1643_785-1641delinsTTG	ENSP00000420412.2:n.785-1643_785-1641deli...
ENST00000489037.2:c.2778_2780delinsTTG	ENSP00000420781.2:p.Phe926=
ENST00000493919.6:c.647-1643_647-1641delinsTTG	ENSP00000418819.2:n.647-1643_647-1641deli...
ENST00000494123.6:c.2856_2858delinsTTG	ENSP00000419103.2:p.Phe952=
ENST00000497488.2:c.1968_1970delinsTTG	ENSP00000418986.2:p.Phe656=
ENST00000618469.2:c.2856_2858delinsTTG	ENSP00000478114.2:p.Phe952=
ENST00000634433.2:c.2733_2735delinsTTG	ENSP00000489431.2:p.Phe911=
ENST00000644379.2:c.2856_2858delinsTTG	ENSP00000496570.2:p.Phe952=
ENST00000644555.2:c.647-1643_647-1641delinsTTG	ENSP00000494614.2:n.647-1643_647-1641deli...
ENST00000652672.2:c.2715_2717delinsTTG	ENSP00000498906.2:p.Phe905=
ENST00000484087.6:c.665-1643_665-1641delinsTTG	ENSP00000419481.2:n.665-1643_665-1641deli...
ENST00000700182.1:c.707-1643_707-1641delinsTTG	ENSP00000514849.1:n.707-1643_707-1641deli...
ENST00000357654.9:c.2856_2858delinsTTG MANE Select	ENSP00000350283.3:p.Phe952=
ENST00000471181.7:c.2856_2858delinsTTG	ENSP00000418960.2:p.Phe952=
ENST00000352993.7:c.671-1643_671-1641delinsTTG	ENSP00000312236.5:n.671-1643_671-1641deli...
ENST00000354071.7:c.2856_2858delinsTTG	ENSP00000326002.7:p.Phe952=
ENST00000357654.7:c.2856_2858delinsTTG	ENSP00000350283.3:p.Phe952=
ENST00000461221.5:c.*2639_*2641delinsTTG	ENSP00000418548.1:n.*2639_*2641delinsTTG
ENST00000468300.5:c.788-1643_788-1641delinsTTG	ENSP00000417148.1:n.788-1643_788-1641deli...
ENST00000471181.6:c.2856_2858delinsTTG	ENSP00000418960.2:p.Phe952=
ENST00000478531.5:c.785-1643_785-1641delinsTTG	ENSP00000420412.1:n.785-1643_785-1641deli...
ENST00000484087.5:c.410-1643_410-1641delinsTTG	ENSP00000419481.1:n.410-1643_410-1641deli...
ENST00000487825.5:c.413-1643_413-1641delinsTTG	ENSP00000418212.1:n.413-1643_413-1641deli...
ENST00000491747.6:c.788-1643_788-1641delinsTTG	ENSP00000420705.2:n.788-1643_788-1641deli...
ENST00000493795.5:c.2715_2717delinsTTG	ENSP00000418775.1:p.Phe905=
ENST00000493919.5:c.647-1643_647-1641delinsTTG	ENSP00000418819.1:n.647-1643_647-1641deli...
ENST00000586385.5:c.5-28724_5-28722delinsTTG	ENSP00000465818.1:n.5-28724_5-28722delins...
ENST00000591534.5:c.-43-18154_-43-18152delinsTTG	ENSP00000467329.1:n.-43-18154_-43-18152de...
ENST00000591849.5:c.-99+32596_-99+32598delinsTTG	ENSP00000465347.1:n.-99+32596_-99+32598de...
NM_007294.3:c.2856_2858delinsTTG , LRG_292t1:c.2856_2858delinsTTG	NP_009225.1:p.Phe952=
NM_007297.3:c.2715_2717delinsTTG	NP_009228.2:p.Phe905=
NM_007298.3:c.788-1643_788-1641delinsTTG	NP_009229.2:n.788-1643_788-1641delinsTTG
NM_007299.3:c.788-1643_788-1641delinsTTG	NP_009230.2:n.788-1643_788-1641delinsTTG
NM_007300.3:c.2856_2858delinsTTG	NP_009231.2:p.Phe952=
NR_027676.1:n.2992_2994delinsTTG
NM_007294.4:c.2856_2858delinsTTG MANE Select	NP_009225.1:p.Phe952=
NM_007297.4:c.2715_2717delinsTTG	NP_009228.2:p.Phe905=
NM_007299.4:c.788-1643_788-1641delinsTTG	NP_009230.2:n.788-1643_788-1641delinsTTG
NM_007300.4:c.2856_2858delinsTTG	NP_009231.2:p.Phe952=
NR_027676.2:n.3033_3035delinsTTG