Canonical Allele Identifier: CA366628279
Gene: BRAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539842G>A , CM000669.2:g.2539842G>A GRCh38
NC_000007.13:g.2579476G>A , CM000669.1:g.2579476G>A GRCh37
NC_000007.12:g.2546002G>A NCBI36
NG_032167.1:g.20917C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1442C>T MANE Select ENSP00000339637.4:p.Ser481Leu
ENST00000340611.8:c.1442C>T ENSP00000339637.4:p.Ser481Leu
ENST00000467558.5:n.2814C>T
ENST00000469750.5:n.4014C>T
ENST00000473879.1:n.158C>T
ENST00000493232.5:n.4178C>T
NM_152743.3:c.1442C>T NP_689956.2:p.Ser481Leu
XM_005249643.3:c.1442C>T XP_005249700.1:p.Ser481Leu
XM_011515177.1:c.1526C>T XP_011513479.1:p.Ser509Leu
XM_011515178.1:c.1526C>T XP_011513480.1:p.Ser509Leu
XM_011515179.1:c.1523C>T XP_011513481.1:p.Ser508Leu
XM_011515180.1:c.1496C>T XP_011513482.1:p.Ser499Leu
XM_011515181.1:c.1526C>T XP_011513483.1:p.Ser509Leu
XM_011515182.1:c.1526C>T XP_011513484.1:p.Ser509Leu
XM_011515183.1:c.1001C>T XP_011513485.1:p.Ser334Leu
XM_011515184.1:c.1001C>T XP_011513486.1:p.Ser334Leu
XM_011515185.1:c.1442C>T XP_011513487.1:p.Ser481Leu
XM_011515186.1:c.1526C>T XP_011513488.1:p.Ser509Leu
XM_011515187.1:c.98C>T XP_011513489.1:p.Ser33Leu
NM_001350626.1:c.1442C>T NP_001337555.1:p.Ser481Leu
NM_001350627.1:c.917C>T NP_001337556.1:p.Ser306Leu
NR_146879.1:n.1859C>T
XM_011515177.2:c.1526C>T XP_011513479.1:p.Ser509Leu
XM_011515179.2:c.1523C>T XP_011513481.1:p.Ser508Leu
XM_011515181.2:c.1526C>T XP_011513483.1:p.Ser509Leu
XM_011515182.2:c.1526C>T XP_011513484.1:p.Ser509Leu
XM_011515184.3:c.1001C>T XP_011513486.1:p.Ser334Leu
XM_011515186.2:c.1526C>T XP_011513488.1:p.Ser509Leu
XM_017011833.1:c.1439C>T XP_016867322.1:p.Ser480Leu
XM_017011834.1:c.1439C>T XP_016867323.1:p.Ser480Leu
XM_017011836.2:c.1442C>T XP_016867325.1:p.Ser481Leu
XM_024446682.1:c.98C>T XP_024302450.1:p.Ser33Leu
NM_152743.4:c.1442C>T MANE Select NP_689956.2:p.Ser481Leu
NM_001350626.2:c.1442C>T NP_001337555.1:p.Ser481Leu
NM_001350627.2:c.917C>T NP_001337556.1:p.Ser306Leu
NR_146879.2:n.1625C>T