Canonical Allele Identifier: CA366628319
Gene: BRAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539851A>G , CM000669.2:g.2539851A>G GRCh38
NC_000007.13:g.2579485A>G , CM000669.1:g.2579485A>G GRCh37
NC_000007.12:g.2546011A>G NCBI36
NG_032167.1:g.20908T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1433T>C MANE Select ENSP00000339637.4:p.Leu478Pro
ENST00000340611.8:c.1433T>C ENSP00000339637.4:p.Leu478Pro
ENST00000467558.5:n.2805T>C
ENST00000469750.5:n.4005T>C
ENST00000473879.1:n.149T>C
ENST00000493232.5:n.4169T>C
NM_152743.3:c.1433T>C NP_689956.2:p.Leu478Pro
XM_005249643.3:c.1433T>C XP_005249700.1:p.Leu478Pro
XM_011515177.1:c.1517T>C XP_011513479.1:p.Leu506Pro
XM_011515178.1:c.1517T>C XP_011513480.1:p.Leu506Pro
XM_011515179.1:c.1514T>C XP_011513481.1:p.Leu505Pro
XM_011515180.1:c.1487T>C XP_011513482.1:p.Leu496Pro
XM_011515181.1:c.1517T>C XP_011513483.1:p.Leu506Pro
XM_011515182.1:c.1517T>C XP_011513484.1:p.Leu506Pro
XM_011515183.1:c.992T>C XP_011513485.1:p.Leu331Pro
XM_011515184.1:c.992T>C XP_011513486.1:p.Leu331Pro
XM_011515185.1:c.1433T>C XP_011513487.1:p.Leu478Pro
XM_011515186.1:c.1517T>C XP_011513488.1:p.Leu506Pro
XM_011515187.1:c.89T>C XP_011513489.1:p.Leu30Pro
NM_001350626.1:c.1433T>C NP_001337555.1:p.Leu478Pro
NM_001350627.1:c.908T>C NP_001337556.1:p.Leu303Pro
NR_146879.1:n.1850T>C
XM_011515177.2:c.1517T>C XP_011513479.1:p.Leu506Pro
XM_011515179.2:c.1514T>C XP_011513481.1:p.Leu505Pro
XM_011515181.2:c.1517T>C XP_011513483.1:p.Leu506Pro
XM_011515182.2:c.1517T>C XP_011513484.1:p.Leu506Pro
XM_011515184.3:c.992T>C XP_011513486.1:p.Leu331Pro
XM_011515186.2:c.1517T>C XP_011513488.1:p.Leu506Pro
XM_017011833.1:c.1430T>C XP_016867322.1:p.Leu477Pro
XM_017011834.1:c.1430T>C XP_016867323.1:p.Leu477Pro
XM_017011836.2:c.1433T>C XP_016867325.1:p.Leu478Pro
XM_024446682.1:c.89T>C XP_024302450.1:p.Leu30Pro
NM_152743.4:c.1433T>C MANE Select NP_689956.2:p.Leu478Pro
NM_001350626.2:c.1433T>C NP_001337555.1:p.Leu478Pro
NM_001350627.2:c.908T>C NP_001337556.1:p.Leu303Pro
NR_146879.2:n.1616T>C