Canonical Allele Identifier: CA366626224
Gene: BRAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539192G>T , CM000669.2:g.2539192G>T GRCh38
NC_000007.13:g.2578826G>T , CM000669.1:g.2578826G>T GRCh37
NC_000007.12:g.2545352G>T NCBI36
NG_032167.1:g.21567C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1757C>A MANE Select ENSP00000339637.4:p.Ala586Glu
ENST00000340611.8:c.1757C>A ENSP00000339637.4:p.Ala586Glu
ENST00000467558.5:n.3129C>A
ENST00000469750.5:n.4329C>A
ENST00000473879.1:n.313+352C>A
ENST00000493232.5:n.4476+352C>A
NM_152743.3:c.1757C>A NP_689956.2:p.Ala586Glu
XM_005249643.3:c.1757C>A XP_005249700.1:p.Ala586Glu
XM_011515177.1:c.1841C>A XP_011513479.1:p.Ala614Glu
XM_011515178.1:c.1841C>A XP_011513480.1:p.Ala614Glu
XM_011515179.1:c.1838C>A XP_011513481.1:p.Ala613Glu
XM_011515180.1:c.1811C>A XP_011513482.1:p.Ala604Glu
XM_011515181.1:c.1841C>A XP_011513483.1:p.Ala614Glu
XM_011515182.1:c.1841C>A XP_011513484.1:p.Ala614Glu
XM_011515183.1:c.1316C>A XP_011513485.1:p.Ala439Glu
XM_011515184.1:c.1316C>A XP_011513486.1:p.Ala439Glu
XM_011515185.1:c.1757C>A XP_011513487.1:p.Ala586Glu
XM_011515186.1:c.1681+352C>A XP_011513488.1:n.1681+352C>A
XM_011515187.1:c.413C>A XP_011513489.1:p.Ala138Glu
NM_001350626.1:c.1757C>A NP_001337555.1:p.Ala586Glu
NM_001350627.1:c.1232C>A NP_001337556.1:p.Ala411Glu
NR_146879.1:n.2174C>A
XM_011515177.2:c.1841C>A XP_011513479.1:p.Ala614Glu
XM_011515179.2:c.1838C>A XP_011513481.1:p.Ala613Glu
XM_011515181.2:c.1841C>A XP_011513483.1:p.Ala614Glu
XM_011515182.2:c.1841C>A XP_011513484.1:p.Ala614Glu
XM_011515184.3:c.1316C>A XP_011513486.1:p.Ala439Glu
XM_011515186.2:c.1681+352C>A XP_011513488.1:n.1681+352C>A
XM_017011833.1:c.1754C>A XP_016867322.1:p.Ala585Glu
XM_017011834.1:c.1754C>A XP_016867323.1:p.Ala585Glu
XM_017011836.2:c.1597+352C>A XP_016867325.1:n.1597+352C>A
XM_024446682.1:c.413C>A XP_024302450.1:p.Ala138Glu
NM_152743.4:c.1757C>A MANE Select NP_689956.2:p.Ala586Glu
NM_001350626.2:c.1757C>A NP_001337555.1:p.Ala586Glu
NM_001350627.2:c.1232C>A NP_001337556.1:p.Ala411Glu
NR_146879.2:n.1940C>A