Canonical Allele Identifier: CA10590509

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 868903
• ClinVar RCV Id: RCV001077894
• dbSNP Id: rs2050983010
• MyVariant Identifiers: chr17:g.41199681T>A (hg19) ; chr17:g.43047664T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43047664T>A , CM000679.2:g.43047664T>A	GRCh38
NC_000017.10:g.41199681T>A , CM000679.1:g.41199681T>A	GRCh37
NC_000017.9:g.38453207T>A	NCBI36
NG_005905.2:g.170320A>T , LRG_292:g.170320A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5443A>T	ENSP00000417241.2:p.Thr1815Ser
ENST00000470026.6:c.5446A>T	ENSP00000419274.2:p.Thr1816Ser
ENST00000473961.6:c.5320A>T	ENSP00000420201.2:p.Thr1774Ser
ENST00000476777.6:c.5440A>T	ENSP00000417554.2:p.Thr1814Ser
ENST00000477152.6:c.5368A>T	ENSP00000419988.2:p.Thr1790Ser
ENST00000478531.6:c.2134A>T	ENSP00000420412.2:p.Thr712Ser
ENST00000489037.2:c.5368A>T	ENSP00000420781.2:p.Thr1790Ser
ENST00000493919.6:c.1996A>T	ENSP00000418819.2:p.Thr666Ser
ENST00000494123.6:c.5446A>T	ENSP00000419103.2:p.Thr1816Ser
ENST00000497488.2:c.4558A>T	ENSP00000418986.2:p.Thr1520Ser
ENST00000618469.2:c.5446A>T	ENSP00000478114.2:p.Thr1816Ser
ENST00000634433.2:c.5323A>T	ENSP00000489431.2:p.Thr1775Ser
ENST00000644379.2:c.5512A>T	ENSP00000496570.2:p.Thr1838Ser
ENST00000644555.2:c.1996A>T	ENSP00000494614.2:p.Thr666Ser
ENST00000652672.2:c.5305A>T	ENSP00000498906.2:p.Thr1769Ser
ENST00000484087.6:c.2008A>T	ENSP00000419481.2:p.Thr670Ser
ENST00000700081.1:n.1329A>T
ENST00000700082.1:n.810A>T
ENST00000357654.9:c.5446A>T MANE Select	ENSP00000350283.3:p.Thr1816Ser
ENST00000471181.7:c.5509A>T	ENSP00000418960.2:p.Thr1837Ser
ENST00000644379.1:c.1833A>T
ENST00000352993.7:c.2020A>T	ENSP00000312236.5:p.Thr674Ser
ENST00000357654.7:c.5446A>T	ENSP00000350283.3:p.Thr1816Ser
ENST00000461221.5:c.*5229A>T	ENSP00000418548.1:n.*5229A>T
ENST00000468300.5:c.2060A>T	ENSP00000417148.1:p.Asp687Val
ENST00000471181.6:c.5509A>T	ENSP00000418960.2:p.Thr1837Ser
ENST00000491747.6:c.2134A>T	ENSP00000420705.2:p.Thr712Ser
ENST00000493795.5:c.5305A>T	ENSP00000418775.1:p.Thr1769Ser
ENST00000586385.5:c.376A>T	ENSP00000465818.1:p.Thr126Ser
ENST00000591534.5:c.919A>T	ENSP00000467329.1:p.Thr307Ser
ENST00000591849.5:c.145A>T	ENSP00000465347.1:p.Thr49Ser
NM_007294.3:c.5446A>T , LRG_292t1:c.5446A>T	NP_009225.1:p.Thr1816Ser
NM_007297.3:c.5305A>T	NP_009228.2:p.Thr1769Ser
NM_007298.3:c.2134A>T	NP_009229.2:p.Thr712Ser
NM_007299.3:c.2060A>T	NP_009230.2:p.Asp687Val
NM_007300.3:c.5509A>T	NP_009231.2:p.Thr1837Ser
NR_027676.1:n.5582A>T
NM_007294.4:c.5446A>T MANE Select	NP_009225.1:p.Thr1816Ser
NM_007297.4:c.5305A>T	NP_009228.2:p.Thr1769Ser
NM_007299.4:c.2060A>T	NP_009230.2:p.Asp687Val
NM_007300.4:c.5509A>T	NP_009231.2:p.Thr1837Ser
NR_027676.2:n.5623A>T