Canonical Allele Identifier: CA2260766450

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43057115_43057116delinsTC , CM000679.2:g.43057115_43057116delinsTC	GRCh38
NC_000017.10:g.41209132_41209133delinsTC , CM000679.1:g.41209132_41209133delinsTC	GRCh37
NC_000017.9:g.38462658_38462659delinsTC	NCBI36
NG_005905.2:g.160868_160869delinsGA , LRG_292:g.160868_160869delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5210_5211delinsGA	ENSP00000417241.2:p.Gly1737=
ENST00000470026.6:c.5213_5214delinsGA	ENSP00000419274.2:p.Gly1738=
ENST00000473961.6:c.5087_5088delinsGA	ENSP00000420201.2:p.Gly1696=
ENST00000476777.6:c.5207_5208delinsGA	ENSP00000417554.2:p.Gly1736=
ENST00000477152.6:c.5135_5136delinsGA	ENSP00000419988.2:p.Gly1712=
ENST00000478531.6:c.1901_1902delinsGA	ENSP00000420412.2:p.Gly634=
ENST00000489037.2:c.5135_5136delinsGA	ENSP00000420781.2:p.Gly1712=
ENST00000493919.6:c.1763_1764delinsGA	ENSP00000418819.2:p.Gly588=
ENST00000494123.6:c.5213_5214delinsGA	ENSP00000419103.2:p.Gly1738=
ENST00000497488.2:c.4325_4326delinsGA	ENSP00000418986.2:p.Gly1442=
ENST00000618469.2:c.5213_5214delinsGA	ENSP00000478114.2:p.Gly1738=
ENST00000634433.2:c.5090_5091delinsGA	ENSP00000489431.2:p.Gly1697=
ENST00000644379.2:c.5279_5280delinsGA	ENSP00000496570.2:p.Gly1760=
ENST00000644555.2:c.1763_1764delinsGA	ENSP00000494614.2:p.Gly588=
ENST00000652672.2:c.5072_5073delinsGA	ENSP00000498906.2:p.Gly1691=
ENST00000484087.6:c.1775_1776delinsGA	ENSP00000419481.2:p.Gly592=
ENST00000357654.9:c.5213_5214delinsGA MANE Select	ENSP00000350283.3:p.Gly1738=
ENST00000471181.7:c.5276_5277delinsGA	ENSP00000418960.2:p.Gly1759=
ENST00000644379.1:c.1600_1601delinsGA
ENST00000352993.7:c.1787_1788delinsGA	ENSP00000312236.5:p.Gly596=
ENST00000357654.7:c.5213_5214delinsGA	ENSP00000350283.3:p.Gly1738=
ENST00000461221.5:c.*4996_*4997delinsGA	ENSP00000418548.1:n.*4996_*4997delinsGA
ENST00000468300.5:c.1901_1902delinsGA	ENSP00000417148.1:p.Gly634=
ENST00000471181.6:c.5276_5277delinsGA	ENSP00000418960.2:p.Gly1759=
ENST00000491747.6:c.1901_1902delinsGA	ENSP00000420705.2:p.Gly634=
ENST00000493795.5:c.5072_5073delinsGA	ENSP00000418775.1:p.Gly1691=
ENST00000586385.5:c.143_144delinsGA	ENSP00000465818.1:p.Gly48=
ENST00000591534.5:c.686_687delinsGA	ENSP00000467329.1:p.Gly229=
ENST00000591849.5:c.-98-6926_-98-6925delinsGA	ENSP00000465347.1:n.-98-6926_-98-6925deli...
NM_007294.3:c.5213_5214delinsGA , LRG_292t1:c.5213_5214delinsGA	NP_009225.1:p.Gly1738=
NM_007297.3:c.5072_5073delinsGA	NP_009228.2:p.Gly1691=
NM_007298.3:c.1901_1902delinsGA	NP_009229.2:p.Gly634=
NM_007299.3:c.1901_1902delinsGA	NP_009230.2:p.Gly634=
NM_007300.3:c.5276_5277delinsGA	NP_009231.2:p.Gly1759=
NR_027676.1:n.5349_5350delinsGA
NM_007294.4:c.5213_5214delinsGA MANE Select	NP_009225.1:p.Gly1738=
NM_007297.4:c.5072_5073delinsGA	NP_009228.2:p.Gly1691=
NM_007299.4:c.1901_1902delinsGA	NP_009230.2:p.Gly634=
NM_007300.4:c.5276_5277delinsGA	NP_009231.2:p.Gly1759=
NR_027676.2:n.5390_5391delinsGA