Canonical Allele Identifier: CA500234108

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41246612G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094595G>T , CM000679.2:g.43094595G>T	GRCh38
NC_000017.10:g.41246612G>T , CM000679.1:g.41246612G>T	GRCh37
NC_000017.9:g.38500138G>T	NCBI36
NG_005905.2:g.123389C>A , LRG_292:g.123389C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1000C>A
ENST00000461574.2:c.936C>A	ENSP00000417241.2:p.Gly312=
ENST00000470026.6:c.936C>A	ENSP00000419274.2:p.Gly312=
ENST00000473961.6:c.810C>A	ENSP00000420201.2:p.Gly270=
ENST00000476777.6:c.933C>A	ENSP00000417554.2:p.Gly311=
ENST00000477152.6:c.858C>A	ENSP00000419988.2:p.Gly286=
ENST00000478531.6:c.784+149C>A	ENSP00000420412.2:n.784+149C>A
ENST00000489037.2:c.858C>A	ENSP00000420781.2:p.Gly286=
ENST00000493919.6:c.646+149C>A	ENSP00000418819.2:n.646+149C>A
ENST00000494123.6:c.936C>A	ENSP00000419103.2:p.Gly312=
ENST00000497488.2:c.48C>A	ENSP00000418986.2:p.Gly16=
ENST00000618469.2:c.936C>A	ENSP00000478114.2:p.Gly312=
ENST00000634433.2:c.813C>A	ENSP00000489431.2:p.Gly271=
ENST00000644379.2:c.936C>A	ENSP00000496570.2:p.Gly312=
ENST00000644555.2:c.646+149C>A	ENSP00000494614.2:n.646+149C>A
ENST00000652672.2:c.795C>A	ENSP00000498906.2:p.Gly265=
ENST00000484087.6:c.664+149C>A	ENSP00000419481.2:n.664+149C>A
ENST00000700182.1:c.706+149C>A	ENSP00000514849.1:n.706+149C>A
ENST00000700183.1:c.*944C>A	ENSP00000514850.1:n.*944C>A
ENST00000357654.9:c.936C>A MANE Select	ENSP00000350283.3:p.Gly312=
ENST00000471181.7:c.936C>A	ENSP00000418960.2:p.Gly312=
ENST00000642945.1:c.*810C>A	ENSP00000495897.1:n.*810C>A
ENST00000652672.1:c.795C>A	ENSP00000498906.1:p.Gly265=
ENST00000352993.7:c.670+1251C>A	ENSP00000312236.5:n.670+1251C>A
ENST00000354071.7:c.936C>A	ENSP00000326002.7:p.Gly312=
ENST00000357654.7:c.936C>A	ENSP00000350283.3:p.Gly312=
ENST00000412061.3:c.287C>A
ENST00000461221.5:c.*719C>A	ENSP00000418548.1:n.*719C>A
ENST00000468300.5:c.787+149C>A	ENSP00000417148.1:n.787+149C>A
ENST00000470026.5:c.936C>A	ENSP00000419274.1:p.Gly312=
ENST00000471181.6:c.936C>A	ENSP00000418960.2:p.Gly312=
ENST00000473961.5:c.533C>A
ENST00000477152.5:c.858C>A	ENSP00000419988.1:p.Gly286=
ENST00000478531.5:c.784+149C>A	ENSP00000420412.1:n.784+149C>A
ENST00000484087.5:c.409+149C>A	ENSP00000419481.1:n.409+149C>A
ENST00000487825.5:c.412+149C>A	ENSP00000418212.1:n.412+149C>A
ENST00000491747.6:c.787+149C>A	ENSP00000420705.2:n.787+149C>A
ENST00000492859.5:c.*872C>A	ENSP00000420253.1:n.*872C>A
ENST00000493795.5:c.795C>A	ENSP00000418775.1:p.Gly265=
ENST00000493919.5:c.646+149C>A	ENSP00000418819.1:n.646+149C>A
ENST00000494123.5:c.936C>A	ENSP00000419103.1:p.Gly312=
ENST00000497488.1:c.48C>A	ENSP00000418986.1:p.Gly16=
ENST00000586385.5:c.4+30587C>A	ENSP00000465818.1:n.4+30587C>A
ENST00000591534.5:c.-43-20074C>A	ENSP00000467329.1:n.-43-20074C>A
ENST00000591849.5:c.-99+30676C>A	ENSP00000465347.1:n.-99+30676C>A
ENST00000634433.1:c.813C>A	ENSP00000489431.1:p.Gly271=
NM_007294.3:c.936C>A , LRG_292t1:c.936C>A	NP_009225.1:p.Gly312=
NM_007297.3:c.795C>A	NP_009228.2:p.Gly265=
NM_007298.3:c.787+149C>A	NP_009229.2:n.787+149C>A
NM_007299.3:c.787+149C>A	NP_009230.2:n.787+149C>A
NM_007300.3:c.936C>A	NP_009231.2:p.Gly312=
NR_027676.1:n.1072C>A
NM_007294.4:c.936C>A MANE Select	NP_009225.1:p.Gly312=
NM_007297.4:c.795C>A	NP_009228.2:p.Gly265=
NM_007299.4:c.787+149C>A	NP_009230.2:n.787+149C>A
NM_007300.4:c.936C>A	NP_009231.2:p.Gly312=
NR_027676.2:n.1113C>A