Canonical Allele Identifier: CA10593253

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41234545C>A (hg19) ; chr17:g.43082528C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082528C>A , CM000679.2:g.43082528C>A	GRCh38
NC_000017.10:g.41234545C>A , CM000679.1:g.41234545C>A	GRCh37
NC_000017.9:g.38488071C>A	NCBI36
NG_005905.2:g.135456G>T , LRG_292:g.135456G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4233G>T	ENSP00000417241.2:p.Met1411Ile
ENST00000470026.6:c.4233G>T	ENSP00000419274.2:p.Met1411Ile
ENST00000473961.6:c.4107G>T	ENSP00000420201.2:p.Met1369Ile
ENST00000476777.6:c.4227G>T	ENSP00000417554.2:p.Met1409Ile
ENST00000477152.6:c.4155G>T	ENSP00000419988.2:p.Met1385Ile
ENST00000478531.6:c.921G>T	ENSP00000420412.2:p.Met307Ile
ENST00000489037.2:c.4155G>T	ENSP00000420781.2:p.Met1385Ile
ENST00000493919.6:c.783G>T	ENSP00000418819.2:p.Met261Ile
ENST00000494123.6:c.4233G>T	ENSP00000419103.2:p.Met1411Ile
ENST00000497488.2:c.3345G>T	ENSP00000418986.2:p.Met1115Ile
ENST00000618469.2:c.4233G>T	ENSP00000478114.2:p.Met1411Ile
ENST00000634433.2:c.4110G>T	ENSP00000489431.2:p.Met1370Ile
ENST00000644379.2:c.4233G>T	ENSP00000496570.2:p.Met1411Ile
ENST00000644555.2:c.783G>T	ENSP00000494614.2:p.Met261Ile
ENST00000652672.2:c.4092G>T	ENSP00000498906.2:p.Met1364Ile
ENST00000484087.6:c.798G>T	ENSP00000419481.2:p.Met266Ile
ENST00000700182.1:c.843G>T	ENSP00000514849.1:p.Met281Ile
ENST00000357654.9:c.4233G>T MANE Select	ENSP00000350283.3:p.Met1411Ile
ENST00000471181.7:c.4233G>T	ENSP00000418960.2:p.Met1411Ile
ENST00000644379.1:c.554G>T
ENST00000352993.7:c.807G>T	ENSP00000312236.5:p.Met269Ile
ENST00000357654.7:c.4233G>T	ENSP00000350283.3:p.Met1411Ile
ENST00000461221.5:c.*4016G>T	ENSP00000418548.1:n.*4016G>T
ENST00000461574.1:c.527G>T
ENST00000468300.5:c.924G>T	ENSP00000417148.1:p.Met308Ile
ENST00000471181.6:c.4233G>T	ENSP00000418960.2:p.Met1411Ile
ENST00000478531.5:c.921G>T	ENSP00000420412.1:p.Met307Ile
ENST00000484087.5:c.546G>T	ENSP00000419481.1:p.Met182Ile
ENST00000487825.5:c.549G>T	ENSP00000418212.1:p.Met183Ile
ENST00000491747.6:c.924G>T	ENSP00000420705.2:p.Met308Ile
ENST00000493795.5:c.4092G>T	ENSP00000418775.1:p.Met1364Ile
ENST00000493919.5:c.783G>T	ENSP00000418819.1:p.Met261Ile
ENST00000586385.5:c.5-18577G>T	ENSP00000465818.1:n.5-18577G>T
ENST00000591534.5:c.-43-8007G>T	ENSP00000467329.1:n.-43-8007G>T
ENST00000591849.5:c.-98-32338G>T	ENSP00000465347.1:n.-98-32338G>T
ENST00000621897.1:n.127G>T
NM_007294.3:c.4233G>T , LRG_292t1:c.4233G>T	NP_009225.1:p.Met1411Ile
NM_007297.3:c.4092G>T	NP_009228.2:p.Met1364Ile
NM_007298.3:c.924G>T	NP_009229.2:p.Met308Ile
NM_007299.3:c.924G>T	NP_009230.2:p.Met308Ile
NM_007300.3:c.4233G>T	NP_009231.2:p.Met1411Ile
NR_027676.1:n.4369G>T
NM_007294.4:c.4233G>T MANE Select	NP_009225.1:p.Met1411Ile
NM_007297.4:c.4092G>T	NP_009228.2:p.Met1364Ile
NM_007299.4:c.924G>T	NP_009230.2:p.Met308Ile
NM_007300.4:c.4233G>T	NP_009231.2:p.Met1411Ile
NR_027676.2:n.4410G>T