Canonical Allele Identifier: CA10591300
Community Standard Title: NM_007294.4(BRCA1):c.5117G>T (p.Gly1706Val)
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43063909C>A , CM000679.2:g.43063909C>A GRCh38
NC_000017.10:g.41215926C>A , CM000679.1:g.41215926C>A GRCh37
NC_000017.9:g.38469452C>A NCBI36
NG_005905.2:g.154075G>T , LRG_292:g.154075G>T

Transcript Alleles

HGVS Amino-acid Change
NM_007294.4:c.5117G>T MANE Select NP_009225.1:p.Gly1706Val
ENST00000357654.9:c.5117G>T MANE Select ENSP00000350283.3:p.Gly1706Val
NM_007294.3:c.5117G>T , LRG_292t1:c.5117G>T NP_009225.1:p.Gly1706Val
NM_007297.3:c.4976G>T NP_009228.2:p.Gly1659Val
NM_007297.4:c.4976G>T NP_009228.2:p.Gly1659Val
NM_007298.3:c.1805G>T NP_009229.2:p.Gly602Val
NM_007299.3:c.1805G>T NP_009230.2:p.Gly602Val
NM_007299.4:c.1805G>T NP_009230.2:p.Gly602Val
NM_007300.3:c.5180G>T NP_009231.2:p.Gly1727Val
NM_007300.4:c.5180G>T NP_009231.2:p.Gly1727Val
NR_027676.1:n.5253G>T
NR_027676.2:n.5294G>T
ENST00000352993.7:c.1691G>T ENSP00000312236.5:p.Gly564Val
ENST00000357654.7:c.5117G>T ENSP00000350283.3:p.Gly1706Val
ENST00000461221.5:c.*4900G>T ENSP00000418548.1:n.*4900G>T
ENST00000461574.2:c.5114G>T ENSP00000417241.2:p.Gly1705Val
ENST00000468300.5:c.1805G>T ENSP00000417148.1:p.Gly602Val
ENST00000470026.6:c.5117G>T ENSP00000419274.2:p.Gly1706Val
ENST00000471181.6:c.5180G>T ENSP00000418960.2:p.Gly1727Val
ENST00000471181.7:c.5180G>T ENSP00000418960.2:p.Gly1727Val
ENST00000473961.6:c.4991G>T ENSP00000420201.2:p.Gly1664Val
ENST00000476777.6:c.5111G>T ENSP00000417554.2:p.Gly1704Val
ENST00000477152.6:c.5039G>T ENSP00000419988.2:p.Gly1680Val
ENST00000478531.5:c.1805G>T ENSP00000420412.1:p.Gly602Val
ENST00000478531.6:c.1805G>T ENSP00000420412.2:p.Gly602Val
ENST00000484087.5:c.1430G>T ENSP00000419481.1:p.Gly477Val
ENST00000484087.6:c.1679G>T ENSP00000419481.2:p.Gly560Val
ENST00000489037.2:c.5039G>T ENSP00000420781.2:p.Gly1680Val
ENST00000491747.6:c.1805G>T ENSP00000420705.2:p.Gly602Val
ENST00000493795.5:c.4976G>T ENSP00000418775.1:p.Gly1659Val
ENST00000493919.5:c.1667G>T ENSP00000418819.1:p.Gly556Val
ENST00000493919.6:c.1667G>T ENSP00000418819.2:p.Gly556Val
ENST00000494123.6:c.5117G>T ENSP00000419103.2:p.Gly1706Val
ENST00000497488.2:c.4229G>T ENSP00000418986.2:p.Gly1410Val
ENST00000586385.5:c.47G>T ENSP00000465818.1:p.Gly16Val
ENST00000591534.5:c.590G>T ENSP00000467329.1:p.Gly197Val
ENST00000591849.5:c.-98-13719G>T ENSP00000465347.1:n.-98-13719G>T
ENST00000618469.2:c.5117G>T ENSP00000478114.2:p.Gly1706Val
ENST00000634433.2:c.4994G>T ENSP00000489431.2:p.Gly1665Val
ENST00000644379.1:c.1504G>T
ENST00000644379.2:c.5183G>T ENSP00000496570.2:p.Gly1728Val
ENST00000644555.2:c.1667G>T ENSP00000494614.2:p.Gly556Val
ENST00000652672.2:c.4976G>T ENSP00000498906.2:p.Gly1659Val