Canonical Allele Identifier: CA10591805

Gene: BRCA1

Linked Data

• dbSNP Id: rs2153830080
• MyVariant Identifiers: chr17:g.41223070C>G (hg19) ; chr17:g.43071053C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071053C>G , CM000679.2:g.43071053C>G	GRCh38
NC_000017.10:g.41223070C>G , CM000679.1:g.41223070C>G	GRCh37
NC_000017.9:g.38476596C>G	NCBI36
NG_005905.2:g.146931G>C , LRG_292:g.146931G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4858G>C	ENSP00000417241.2:p.Asp1620His
ENST00000470026.6:c.4861G>C	ENSP00000419274.2:p.Asp1621His
ENST00000473961.6:c.4735G>C	ENSP00000420201.2:p.Asp1579His
ENST00000476777.6:c.4855G>C	ENSP00000417554.2:p.Asp1619His
ENST00000477152.6:c.4783G>C	ENSP00000419988.2:p.Asp1595His
ENST00000478531.6:c.1549G>C	ENSP00000420412.2:p.Asp517His
ENST00000489037.2:c.4783G>C	ENSP00000420781.2:p.Asp1595His
ENST00000493919.6:c.1411G>C	ENSP00000418819.2:p.Asp471His
ENST00000494123.6:c.4861G>C	ENSP00000419103.2:p.Asp1621His
ENST00000497488.2:c.3973G>C	ENSP00000418986.2:p.Asp1325His
ENST00000618469.2:c.4861G>C	ENSP00000478114.2:p.Asp1621His
ENST00000634433.2:c.4738G>C	ENSP00000489431.2:p.Asp1580His
ENST00000644379.2:c.4927G>C	ENSP00000496570.2:p.Asp1643His
ENST00000644555.2:c.1411G>C	ENSP00000494614.2:p.Asp471His
ENST00000652672.2:c.4720G>C	ENSP00000498906.2:p.Asp1574His
ENST00000484087.6:c.1423G>C	ENSP00000419481.2:p.Asp475His
ENST00000700182.1:c.1468G>C	ENSP00000514849.1:p.Asp490His
ENST00000357654.9:c.4861G>C MANE Select	ENSP00000350283.3:p.Asp1621His
ENST00000471181.7:c.4924G>C	ENSP00000418960.2:p.Asp1642His
ENST00000644379.1:c.1248G>C
ENST00000352993.7:c.1435G>C	ENSP00000312236.5:p.Asp479His
ENST00000357654.7:c.4861G>C	ENSP00000350283.3:p.Asp1621His
ENST00000461221.5:c.*4644G>C	ENSP00000418548.1:n.*4644G>C
ENST00000468300.5:c.1549G>C	ENSP00000417148.1:p.Asp517His
ENST00000471181.6:c.4924G>C	ENSP00000418960.2:p.Asp1642His
ENST00000472490.1:n.14G>C
ENST00000478531.5:c.1549G>C	ENSP00000420412.1:p.Asp517His
ENST00000484087.5:c.1174G>C	ENSP00000419481.1:p.Asp392His
ENST00000491747.6:c.1549G>C	ENSP00000420705.2:p.Asp517His
ENST00000493795.5:c.4720G>C	ENSP00000418775.1:p.Asp1574His
ENST00000493919.5:c.1411G>C	ENSP00000418819.1:p.Asp471His
ENST00000586385.5:c.5-7102G>C	ENSP00000465818.1:n.5-7102G>C
ENST00000591534.5:c.334G>C	ENSP00000467329.1:p.Asp112His
ENST00000591849.5:c.-98-20863G>C	ENSP00000465347.1:n.-98-20863G>C
NM_007294.3:c.4861G>C , LRG_292t1:c.4861G>C	NP_009225.1:p.Asp1621His
NM_007297.3:c.4720G>C	NP_009228.2:p.Asp1574His
NM_007298.3:c.1549G>C	NP_009229.2:p.Asp517His
NM_007299.3:c.1549G>C	NP_009230.2:p.Asp517His
NM_007300.3:c.4924G>C	NP_009231.2:p.Asp1642His
NR_027676.1:n.4997G>C
NM_007294.4:c.4861G>C MANE Select	NP_009225.1:p.Asp1621His
NM_007297.4:c.4720G>C	NP_009228.2:p.Asp1574His
NM_007299.4:c.1549G>C	NP_009230.2:p.Asp517His
NM_007300.4:c.4924G>C	NP_009231.2:p.Asp1642His
NR_027676.2:n.5038G>C