Canonical Allele Identifier: CA10591340
Community Standard Title: NM_007294.4(BRCA1):c.5092G>T (p.Glu1698Ter)
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43063934C>A , CM000679.2:g.43063934C>A GRCh38
NC_000017.10:g.41215951C>A , CM000679.1:g.41215951C>A GRCh37
NC_000017.9:g.38469477C>A NCBI36
NG_005905.2:g.154050G>T , LRG_292:g.154050G>T

Transcript Alleles

HGVS Amino-acid Change
NM_007294.4:c.5092G>T MANE Select NP_009225.1:p.Glu1698Ter
ENST00000357654.9:c.5092G>T MANE Select ENSP00000350283.3:p.Glu1698Ter
NM_007294.3:c.5092G>T , LRG_292t1:c.5092G>T NP_009225.1:p.Glu1698Ter
NM_007297.3:c.4951G>T NP_009228.2:p.Glu1651Ter
NM_007297.4:c.4951G>T NP_009228.2:p.Glu1651Ter
NM_007298.3:c.1780G>T NP_009229.2:p.Glu594Ter
NM_007299.3:c.1780G>T NP_009230.2:p.Glu594Ter
NM_007299.4:c.1780G>T NP_009230.2:p.Glu594Ter
NM_007300.3:c.5155G>T NP_009231.2:p.Glu1719Ter
NM_007300.4:c.5155G>T NP_009231.2:p.Glu1719Ter
NR_027676.1:n.5228G>T
NR_027676.2:n.5269G>T
ENST00000352993.7:c.1666G>T ENSP00000312236.5:p.Glu556Ter
ENST00000357654.7:c.5092G>T ENSP00000350283.3:p.Glu1698Ter
ENST00000461221.5:c.*4875G>T ENSP00000418548.1:n.*4875G>T
ENST00000461574.2:c.5089G>T ENSP00000417241.2:p.Glu1697Ter
ENST00000468300.5:c.1780G>T ENSP00000417148.1:p.Glu594Ter
ENST00000470026.6:c.5092G>T ENSP00000419274.2:p.Glu1698Ter
ENST00000471181.6:c.5155G>T ENSP00000418960.2:p.Glu1719Ter
ENST00000471181.7:c.5155G>T ENSP00000418960.2:p.Glu1719Ter
ENST00000473961.6:c.4966G>T ENSP00000420201.2:p.Glu1656Ter
ENST00000476777.6:c.5086G>T ENSP00000417554.2:p.Glu1696Ter
ENST00000477152.6:c.5014G>T ENSP00000419988.2:p.Glu1672Ter
ENST00000478531.5:c.1780G>T ENSP00000420412.1:p.Glu594Ter
ENST00000478531.6:c.1780G>T ENSP00000420412.2:p.Glu594Ter
ENST00000484087.5:c.1405G>T ENSP00000419481.1:p.Glu469Ter
ENST00000484087.6:c.1654G>T ENSP00000419481.2:p.Glu552Ter
ENST00000489037.2:c.5014G>T ENSP00000420781.2:p.Glu1672Ter
ENST00000491747.6:c.1780G>T ENSP00000420705.2:p.Glu594Ter
ENST00000493795.5:c.4951G>T ENSP00000418775.1:p.Glu1651Ter
ENST00000493919.5:c.1642G>T ENSP00000418819.1:p.Glu548Ter
ENST00000493919.6:c.1642G>T ENSP00000418819.2:p.Glu548Ter
ENST00000494123.6:c.5092G>T ENSP00000419103.2:p.Glu1698Ter
ENST00000497488.2:c.4204G>T ENSP00000418986.2:p.Glu1402Ter
ENST00000586385.5:c.22G>T ENSP00000465818.1:p.Glu8Ter
ENST00000591534.5:c.565G>T ENSP00000467329.1:p.Glu189Ter
ENST00000591849.5:c.-98-13744G>T ENSP00000465347.1:n.-98-13744G>T
ENST00000618469.2:c.5092G>T ENSP00000478114.2:p.Glu1698Ter
ENST00000634433.2:c.4969G>T ENSP00000489431.2:p.Glu1657Ter
ENST00000644379.1:c.1479G>T
ENST00000644379.2:c.5158G>T ENSP00000496570.2:p.Glu1720Ter
ENST00000644555.2:c.1642G>T ENSP00000494614.2:p.Glu548Ter
ENST00000652672.2:c.4951G>T ENSP00000498906.2:p.Glu1651Ter