Canonical Allele Identifier: CA366628396
Gene: BRAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539876C>G , CM000669.2:g.2539876C>G GRCh38
NC_000007.13:g.2579510C>G , CM000669.1:g.2579510C>G GRCh37
NC_000007.12:g.2546036C>G NCBI36
NG_032167.1:g.20883G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1408G>C MANE Select ENSP00000339637.4:p.Ala470Pro
ENST00000340611.8:c.1408G>C ENSP00000339637.4:p.Ala470Pro
ENST00000467558.5:n.2780G>C
ENST00000469750.5:n.3980G>C
ENST00000473879.1:n.124G>C
ENST00000493232.5:n.4144G>C
NM_152743.3:c.1408G>C NP_689956.2:p.Ala470Pro
XM_005249643.3:c.1408G>C XP_005249700.1:p.Ala470Pro
XM_011515177.1:c.1492G>C XP_011513479.1:p.Ala498Pro
XM_011515178.1:c.1492G>C XP_011513480.1:p.Ala498Pro
XM_011515179.1:c.1489G>C XP_011513481.1:p.Ala497Pro
XM_011515180.1:c.1462G>C XP_011513482.1:p.Ala488Pro
XM_011515181.1:c.1492G>C XP_011513483.1:p.Ala498Pro
XM_011515182.1:c.1492G>C XP_011513484.1:p.Ala498Pro
XM_011515183.1:c.967G>C XP_011513485.1:p.Ala323Pro
XM_011515184.1:c.967G>C XP_011513486.1:p.Ala323Pro
XM_011515185.1:c.1408G>C XP_011513487.1:p.Ala470Pro
XM_011515186.1:c.1492G>C XP_011513488.1:p.Ala498Pro
XM_011515187.1:c.64G>C XP_011513489.1:p.Ala22Pro
NM_001350626.1:c.1408G>C NP_001337555.1:p.Ala470Pro
NM_001350627.1:c.883G>C NP_001337556.1:p.Ala295Pro
NR_146879.1:n.1825G>C
XM_011515177.2:c.1492G>C XP_011513479.1:p.Ala498Pro
XM_011515179.2:c.1489G>C XP_011513481.1:p.Ala497Pro
XM_011515181.2:c.1492G>C XP_011513483.1:p.Ala498Pro
XM_011515182.2:c.1492G>C XP_011513484.1:p.Ala498Pro
XM_011515184.3:c.967G>C XP_011513486.1:p.Ala323Pro
XM_011515186.2:c.1492G>C XP_011513488.1:p.Ala498Pro
XM_017011833.1:c.1405G>C XP_016867322.1:p.Ala469Pro
XM_017011834.1:c.1405G>C XP_016867323.1:p.Ala469Pro
XM_017011836.2:c.1408G>C XP_016867325.1:p.Ala470Pro
XM_024446682.1:c.64G>C XP_024302450.1:p.Ala22Pro
NM_152743.4:c.1408G>C MANE Select NP_689956.2:p.Ala470Pro
NM_001350626.2:c.1408G>C NP_001337555.1:p.Ala470Pro
NM_001350627.2:c.883G>C NP_001337556.1:p.Ala295Pro
NR_146879.2:n.1591G>C