Canonical Allele Identifier: CA2695225931

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082403_43082404insA , CM000679.2:g.43082403_43082404insA	GRCh38
NC_000017.10:g.41234420_41234421insA , CM000679.1:g.41234420_41234421insA	GRCh37
NC_000017.9:g.38487946_38487947insA	NCBI36
NG_005905.2:g.135580_135581insT , LRG_292:g.135580_135581insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4357_4357+1insT	ENSP00000417241.2:n.4357_4357+1insT
ENST00000470026.6:c.4357_4357+1insT	ENSP00000419274.2:n.4357_4357+1insT
ENST00000473961.6:c.4231_4231+1insT	ENSP00000420201.2:n.4231_4231+1insT
ENST00000476777.6:c.4351_4351+1insT	ENSP00000417554.2:n.4351_4351+1insT
ENST00000477152.6:c.4279_4279+1insT	ENSP00000419988.2:n.4279_4279+1insT
ENST00000478531.6:c.1045_1045+1insT	ENSP00000420412.2:n.1045_1045+1insT
ENST00000489037.2:c.4279_4279+1insT	ENSP00000420781.2:n.4279_4279+1insT
ENST00000493919.6:c.907_907+1insT	ENSP00000418819.2:n.907_907+1insT
ENST00000494123.6:c.4357_4357+1insT	ENSP00000419103.2:n.4357_4357+1insT
ENST00000497488.2:c.3469_3469+1insT	ENSP00000418986.2:n.3469_3469+1insT
ENST00000618469.2:c.4357_4357+1insT	ENSP00000478114.2:n.4357_4357+1insT
ENST00000634433.2:c.4234_4234+1insT	ENSP00000489431.2:n.4234_4234+1insT
ENST00000644379.2:c.4357_4357+1insT	ENSP00000496570.2:n.4357_4357+1insT
ENST00000644555.2:c.907_907+1insT	ENSP00000494614.2:n.907_907+1insT
ENST00000652672.2:c.4216_4216+1insT	ENSP00000498906.2:n.4216_4216+1insT
ENST00000484087.6:c.922_922+1insT	ENSP00000419481.2:n.922_922+1insT
ENST00000700182.1:c.967_967+1insT	ENSP00000514849.1:n.967_967+1insT
ENST00000357654.9:c.4357_4357+1insT MANE Select	ENSP00000350283.3:n.4357_4357+1insT
ENST00000471181.7:c.4357_4357+1insT	ENSP00000418960.2:n.4357_4357+1insT
ENST00000644379.1:c.678_678+1insT
ENST00000352993.7:c.931_931+1insT	ENSP00000312236.5:n.931_931+1insT
ENST00000357654.7:c.4357_4357+1insT	ENSP00000350283.3:n.4357_4357+1insT
ENST00000461221.5:c.*4140_*4140+1insT	ENSP00000418548.1:n.*4140_*4140+1insT
ENST00000461574.1:c.651_651+1insT
ENST00000468300.5:c.1048_1048+1insT	ENSP00000417148.1:n.1048_1048+1insT
ENST00000471181.6:c.4357_4357+1insT	ENSP00000418960.2:n.4357_4357+1insT
ENST00000478531.5:c.1045_1045+1insT	ENSP00000420412.1:n.1045_1045+1insT
ENST00000484087.5:c.670_670+1insT	ENSP00000419481.1:n.670_670+1insT
ENST00000487825.5:c.673_673+1insT	ENSP00000418212.1:n.673_673+1insT
ENST00000491747.6:c.1048_1048+1insT	ENSP00000420705.2:n.1048_1048+1insT
ENST00000493795.5:c.4216_4216+1insT	ENSP00000418775.1:n.4216_4216+1insT
ENST00000493919.5:c.907_907+1insT	ENSP00000418819.1:n.907_907+1insT
ENST00000586385.5:c.5-18453_5-18452insT	ENSP00000465818.1:n.5-18453_5-18452insT
ENST00000591534.5:c.-43-7883_-43-7882insT	ENSP00000467329.1:n.-43-7883_-43-7882insT
ENST00000591849.5:c.-98-32214_-98-32213insT	ENSP00000465347.1:n.-98-32214_-98-32213insT
ENST00000621897.1:n.251_251+1insT
NM_007294.3:c.4357_4357+1insT , LRG_292t1:c.4357_4357+1insT	NP_009225.1:n.4357_4357+1insT
NM_007297.3:c.4216_4216+1insT	NP_009228.2:n.4216_4216+1insT
NM_007298.3:c.1048_1048+1insT	NP_009229.2:n.1048_1048+1insT
NM_007299.3:c.1048_1048+1insT	NP_009230.2:n.1048_1048+1insT
NM_007300.3:c.4357_4357+1insT	NP_009231.2:n.4357_4357+1insT
NR_027676.1:n.4493_4493+1insT
NM_007294.4:c.4357_4357+1insT MANE Select	NP_009225.1:n.4357_4357+1insT
NM_007297.4:c.4216_4216+1insT	NP_009228.2:n.4216_4216+1insT
NM_007299.4:c.1048_1048+1insT	NP_009230.2:n.1048_1048+1insT
NM_007300.4:c.4357_4357+1insT	NP_009231.2:n.4357_4357+1insT
NR_027676.2:n.4534_4534+1insT