Canonical Allele Identifier: CA500233172

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41245588_41245589insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093571_43093572insA , CM000679.2:g.43093571_43093572insA	GRCh38
NC_000017.10:g.41245588_41245589insA , CM000679.1:g.41245588_41245589insA	GRCh37
NC_000017.9:g.38499114_38499115insA	NCBI36
NG_005905.2:g.124412_124413insT , LRG_292:g.124412_124413insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2023_2024insT
ENST00000461574.2:c.1959_1960insT	ENSP00000417241.2:p.Lys654Ter
ENST00000470026.6:c.1959_1960insT	ENSP00000419274.2:p.Lys654Ter
ENST00000473961.6:c.1833_1834insT	ENSP00000420201.2:p.Lys612Ter
ENST00000476777.6:c.1956_1957insT	ENSP00000417554.2:p.Lys653Ter
ENST00000477152.6:c.1881_1882insT	ENSP00000419988.2:p.Lys628Ter
ENST00000478531.6:c.784+1172_784+1173insT	ENSP00000420412.2:n.784+1172_784+1173insT
ENST00000489037.2:c.1881_1882insT	ENSP00000420781.2:p.Lys628Ter
ENST00000493919.6:c.646+1172_646+1173insT	ENSP00000418819.2:n.646+1172_646+1173insT
ENST00000494123.6:c.1959_1960insT	ENSP00000419103.2:p.Lys654Ter
ENST00000497488.2:c.1071_1072insT	ENSP00000418986.2:p.Lys358Ter
ENST00000618469.2:c.1959_1960insT	ENSP00000478114.2:p.Lys654Ter
ENST00000634433.2:c.1836_1837insT	ENSP00000489431.2:p.Lys613Ter
ENST00000644379.2:c.1959_1960insT	ENSP00000496570.2:p.Lys654Ter
ENST00000644555.2:c.646+1172_646+1173insT	ENSP00000494614.2:n.646+1172_646+1173insT
ENST00000652672.2:c.1818_1819insT	ENSP00000498906.2:p.Lys607Ter
ENST00000484087.6:c.664+1172_664+1173insT	ENSP00000419481.2:n.664+1172_664+1173insT
ENST00000700182.1:c.706+1172_706+1173insT	ENSP00000514849.1:n.706+1172_706+1173insT
ENST00000357654.9:c.1959_1960insT MANE Select	ENSP00000350283.3:p.Lys654Ter
ENST00000471181.7:c.1959_1960insT	ENSP00000418960.2:p.Lys654Ter
ENST00000352993.7:c.670+2274_670+2275insT	ENSP00000312236.5:n.670+2274_670+2275insT
ENST00000354071.7:c.1959_1960insT	ENSP00000326002.7:p.Lys654Ter
ENST00000357654.7:c.1959_1960insT	ENSP00000350283.3:p.Lys654Ter
ENST00000412061.3:c.1310_1311insT
ENST00000461221.5:c.*1742_*1743insT	ENSP00000418548.1:n.*1742_*1743insT
ENST00000468300.5:c.787+1172_787+1173insT	ENSP00000417148.1:n.787+1172_787+1173insT
ENST00000471181.6:c.1959_1960insT	ENSP00000418960.2:p.Lys654Ter
ENST00000478531.5:c.784+1172_784+1173insT	ENSP00000420412.1:n.784+1172_784+1173insT
ENST00000484087.5:c.409+1172_409+1173insT	ENSP00000419481.1:n.409+1172_409+1173insT
ENST00000487825.5:c.412+1172_412+1173insT	ENSP00000418212.1:n.412+1172_412+1173insT
ENST00000491747.6:c.787+1172_787+1173insT	ENSP00000420705.2:n.787+1172_787+1173insT
ENST00000493795.5:c.1818_1819insT	ENSP00000418775.1:p.Lys607Ter
ENST00000493919.5:c.646+1172_646+1173insT	ENSP00000418819.1:n.646+1172_646+1173insT
ENST00000586385.5:c.5-29621_5-29620insT	ENSP00000465818.1:n.5-29621_5-29620insT
ENST00000591534.5:c.-43-19051_-43-19050insT	ENSP00000467329.1:n.-43-19051_-43-19050insT
ENST00000591849.5:c.-99+31699_-99+31700insT	ENSP00000465347.1:n.-99+31699_-99+31700insT
ENST00000634433.1:c.1836_1837insT	ENSP00000489431.1:p.Lys613Ter
NM_007294.3:c.1959_1960insT , LRG_292t1:c.1959_1960insT	NP_009225.1:p.Lys654Ter
NM_007297.3:c.1818_1819insT	NP_009228.2:p.Lys607Ter
NM_007298.3:c.787+1172_787+1173insT	NP_009229.2:n.787+1172_787+1173insT
NM_007299.3:c.787+1172_787+1173insT	NP_009230.2:n.787+1172_787+1173insT
NM_007300.3:c.1959_1960insT	NP_009231.2:p.Lys654Ter
NR_027676.1:n.2095_2096insT
NM_007294.4:c.1959_1960insT MANE Select	NP_009225.1:p.Lys654Ter
NM_007297.4:c.1818_1819insT	NP_009228.2:p.Lys607Ter
NM_007299.4:c.787+1172_787+1173insT	NP_009230.2:n.787+1172_787+1173insT
NM_007300.4:c.1959_1960insT	NP_009231.2:p.Lys654Ter
NR_027676.2:n.2136_2137insT