Canonical Allele Identifier: CA1683198907
Gene: BRAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539120A= , CM000669.2:g.2539120A= GRCh38
NC_000007.13:g.2578754A= , CM000669.1:g.2578754A= GRCh37
NC_000007.12:g.2545280A= NCBI36
NG_032167.1:g.21639T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1770+59T= MANE Select ENSP00000339637.4:n.1770+59T=
ENST00000340611.8:c.1770+59T= ENSP00000339637.4:n.1770+59T=
ENST00000467558.5:n.3201T=
ENST00000469750.5:n.4342+59T=
ENST00000473879.1:n.314-356T=
ENST00000493232.5:n.4477-356T=
NM_152743.3:c.1770+59T= NP_689956.2:n.1770+59T=
XM_005249643.3:c.1770+59T= XP_005249700.1:n.1770+59T=
XM_011515177.1:c.1854+59T= XP_011513479.1:n.1854+59T=
XM_011515178.1:c.1854+59T= XP_011513480.1:n.1854+59T=
XM_011515179.1:c.1851+59T= XP_011513481.1:n.1851+59T=
XM_011515180.1:c.1824+59T= XP_011513482.1:n.1824+59T=
XM_011515181.1:c.1854+59T= XP_011513483.1:n.1854+59T=
XM_011515182.1:c.1854+59T= XP_011513484.1:n.1854+59T=
XM_011515183.1:c.1329+59T= XP_011513485.1:n.1329+59T=
XM_011515184.1:c.1329+59T= XP_011513486.1:n.1329+59T=
XM_011515185.1:c.1770+59T= XP_011513487.1:n.1770+59T=
XM_011515186.1:c.1682-356T= XP_011513488.1:n.1682-356T=
XM_011515187.1:c.426+59T= XP_011513489.1:n.426+59T=
NM_001350626.1:c.1770+59T= NP_001337555.1:n.1770+59T=
NM_001350627.1:c.1245+59T= NP_001337556.1:n.1245+59T=
NR_146879.1:n.2187+59T=
XM_011515177.2:c.1854+59T= XP_011513479.1:n.1854+59T=
XM_011515179.2:c.1851+59T= XP_011513481.1:n.1851+59T=
XM_011515181.2:c.1854+59T= XP_011513483.1:n.1854+59T=
XM_011515182.2:c.1854+59T= XP_011513484.1:n.1854+59T=
XM_011515184.3:c.1329+59T= XP_011513486.1:n.1329+59T=
XM_011515186.2:c.1682-356T= XP_011513488.1:n.1682-356T=
XM_017011833.1:c.1767+59T= XP_016867322.1:n.1767+59T=
XM_017011834.1:c.1767+59T= XP_016867323.1:n.1767+59T=
XM_017011836.2:c.1598-356T= XP_016867325.1:n.1598-356T=
XM_024446682.1:c.426+59T= XP_024302450.1:n.426+59T=
NM_152743.4:c.1770+59T= MANE Select NP_689956.2:n.1770+59T=
NM_001350626.2:c.1770+59T= NP_001337555.1:n.1770+59T=
NM_001350627.2:c.1245+59T= NP_001337556.1:n.1245+59T=
NR_146879.2:n.1953+59T=