Canonical Allele Identifier: CA366628360
Gene: BRAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539860A>T , CM000669.2:g.2539860A>T GRCh38
NC_000007.13:g.2579494A>T , CM000669.1:g.2579494A>T GRCh37
NC_000007.12:g.2546020A>T NCBI36
NG_032167.1:g.20899T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1424T>A MANE Select ENSP00000339637.4:p.Leu475His
ENST00000340611.8:c.1424T>A ENSP00000339637.4:p.Leu475His
ENST00000467558.5:n.2796T>A
ENST00000469750.5:n.3996T>A
ENST00000473879.1:n.140T>A
ENST00000493232.5:n.4160T>A
NM_152743.3:c.1424T>A NP_689956.2:p.Leu475His
XM_005249643.3:c.1424T>A XP_005249700.1:p.Leu475His
XM_011515177.1:c.1508T>A XP_011513479.1:p.Leu503His
XM_011515178.1:c.1508T>A XP_011513480.1:p.Leu503His
XM_011515179.1:c.1505T>A XP_011513481.1:p.Leu502His
XM_011515180.1:c.1478T>A XP_011513482.1:p.Leu493His
XM_011515181.1:c.1508T>A XP_011513483.1:p.Leu503His
XM_011515182.1:c.1508T>A XP_011513484.1:p.Leu503His
XM_011515183.1:c.983T>A XP_011513485.1:p.Leu328His
XM_011515184.1:c.983T>A XP_011513486.1:p.Leu328His
XM_011515185.1:c.1424T>A XP_011513487.1:p.Leu475His
XM_011515186.1:c.1508T>A XP_011513488.1:p.Leu503His
XM_011515187.1:c.80T>A XP_011513489.1:p.Leu27His
NM_001350626.1:c.1424T>A NP_001337555.1:p.Leu475His
NM_001350627.1:c.899T>A NP_001337556.1:p.Leu300His
NR_146879.1:n.1841T>A
XM_011515177.2:c.1508T>A XP_011513479.1:p.Leu503His
XM_011515179.2:c.1505T>A XP_011513481.1:p.Leu502His
XM_011515181.2:c.1508T>A XP_011513483.1:p.Leu503His
XM_011515182.2:c.1508T>A XP_011513484.1:p.Leu503His
XM_011515184.3:c.983T>A XP_011513486.1:p.Leu328His
XM_011515186.2:c.1508T>A XP_011513488.1:p.Leu503His
XM_017011833.1:c.1421T>A XP_016867322.1:p.Leu474His
XM_017011834.1:c.1421T>A XP_016867323.1:p.Leu474His
XM_017011836.2:c.1424T>A XP_016867325.1:p.Leu475His
XM_024446682.1:c.80T>A XP_024302450.1:p.Leu27His
NM_152743.4:c.1424T>A MANE Select NP_689956.2:p.Leu475His
NM_001350626.2:c.1424T>A NP_001337555.1:p.Leu475His
NM_001350627.2:c.899T>A NP_001337556.1:p.Leu300His
NR_146879.2:n.1607T>A