Canonical Allele Identifier: CA366628298
Gene: BRAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539846T>A , CM000669.2:g.2539846T>A GRCh38
NC_000007.13:g.2579480T>A , CM000669.1:g.2579480T>A GRCh37
NC_000007.12:g.2546006T>A NCBI36
NG_032167.1:g.20913A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1438A>T MANE Select ENSP00000339637.4:p.Ser480Cys
ENST00000340611.8:c.1438A>T ENSP00000339637.4:p.Ser480Cys
ENST00000467558.5:n.2810A>T
ENST00000469750.5:n.4010A>T
ENST00000473879.1:n.154A>T
ENST00000493232.5:n.4174A>T
NM_152743.3:c.1438A>T NP_689956.2:p.Ser480Cys
XM_005249643.3:c.1438A>T XP_005249700.1:p.Ser480Cys
XM_011515177.1:c.1522A>T XP_011513479.1:p.Ser508Cys
XM_011515178.1:c.1522A>T XP_011513480.1:p.Ser508Cys
XM_011515179.1:c.1519A>T XP_011513481.1:p.Ser507Cys
XM_011515180.1:c.1492A>T XP_011513482.1:p.Ser498Cys
XM_011515181.1:c.1522A>T XP_011513483.1:p.Ser508Cys
XM_011515182.1:c.1522A>T XP_011513484.1:p.Ser508Cys
XM_011515183.1:c.997A>T XP_011513485.1:p.Ser333Cys
XM_011515184.1:c.997A>T XP_011513486.1:p.Ser333Cys
XM_011515185.1:c.1438A>T XP_011513487.1:p.Ser480Cys
XM_011515186.1:c.1522A>T XP_011513488.1:p.Ser508Cys
XM_011515187.1:c.94A>T XP_011513489.1:p.Ser32Cys
NM_001350626.1:c.1438A>T NP_001337555.1:p.Ser480Cys
NM_001350627.1:c.913A>T NP_001337556.1:p.Ser305Cys
NR_146879.1:n.1855A>T
XM_011515177.2:c.1522A>T XP_011513479.1:p.Ser508Cys
XM_011515179.2:c.1519A>T XP_011513481.1:p.Ser507Cys
XM_011515181.2:c.1522A>T XP_011513483.1:p.Ser508Cys
XM_011515182.2:c.1522A>T XP_011513484.1:p.Ser508Cys
XM_011515184.3:c.997A>T XP_011513486.1:p.Ser333Cys
XM_011515186.2:c.1522A>T XP_011513488.1:p.Ser508Cys
XM_017011833.1:c.1435A>T XP_016867322.1:p.Ser479Cys
XM_017011834.1:c.1435A>T XP_016867323.1:p.Ser479Cys
XM_017011836.2:c.1438A>T XP_016867325.1:p.Ser480Cys
XM_024446682.1:c.94A>T XP_024302450.1:p.Ser32Cys
NM_152743.4:c.1438A>T MANE Select NP_689956.2:p.Ser480Cys
NM_001350626.2:c.1438A>T NP_001337555.1:p.Ser480Cys
NM_001350627.2:c.913A>T NP_001337556.1:p.Ser305Cys
NR_146879.2:n.1621A>T