Canonical Allele Identifier: CA1683199369
Gene: BRAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2539899T= , CM000669.2:g.2539899T= GRCh38
NC_000007.13:g.2579533T= , CM000669.1:g.2579533T= GRCh37
NC_000007.12:g.2546059T= NCBI36
NG_032167.1:g.20860A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340611.9:c.1396-11A= MANE Select ENSP00000339637.4:n.1396-11A=
ENST00000340611.8:c.1396-11A= ENSP00000339637.4:n.1396-11A=
ENST00000467558.5:n.2757A=
ENST00000469750.5:n.3957A=
ENST00000473879.1:n.112-11A=
ENST00000493232.5:n.4121A=
NM_152743.3:c.1396-11A= NP_689956.2:n.1396-11A=
XM_005249643.3:c.1396-11A= XP_005249700.1:n.1396-11A=
XM_011515177.1:c.1469A= XP_011513479.1:p.Tyr490=
XM_011515178.1:c.1469A= XP_011513480.1:p.Tyr490=
XM_011515179.1:c.1466A= XP_011513481.1:p.Tyr489=
XM_011515180.1:c.1439A= XP_011513482.1:p.Tyr480=
XM_011515181.1:c.1469A= XP_011513483.1:p.Tyr490=
XM_011515182.1:c.1469A= XP_011513484.1:p.Tyr490=
XM_011515183.1:c.944A= XP_011513485.1:p.Tyr315=
XM_011515184.1:c.944A= XP_011513486.1:p.Tyr315=
XM_011515185.1:c.1396-11A= XP_011513487.1:n.1396-11A=
XM_011515186.1:c.1469A= XP_011513488.1:p.Tyr490=
XM_011515187.1:c.52-11A= XP_011513489.1:n.52-11A=
NM_001350626.1:c.1396-11A= NP_001337555.1:n.1396-11A=
NM_001350627.1:c.871-11A= NP_001337556.1:n.871-11A=
NR_146879.1:n.1813-11A=
XM_011515177.2:c.1469A= XP_011513479.1:p.Tyr490=
XM_011515179.2:c.1466A= XP_011513481.1:p.Tyr489=
XM_011515181.2:c.1469A= XP_011513483.1:p.Tyr490=
XM_011515182.2:c.1469A= XP_011513484.1:p.Tyr490=
XM_011515184.3:c.944A= XP_011513486.1:p.Tyr315=
XM_011515186.2:c.1469A= XP_011513488.1:p.Tyr490=
XM_017011833.1:c.1393-11A= XP_016867322.1:n.1393-11A=
XM_017011834.1:c.1393-11A= XP_016867323.1:n.1393-11A=
XM_017011836.2:c.1396-11A= XP_016867325.1:n.1396-11A=
XM_024446682.1:c.52-11A= XP_024302450.1:n.52-11A=
NM_152743.4:c.1396-11A= MANE Select NP_689956.2:n.1396-11A=
NM_001350626.2:c.1396-11A= NP_001337555.1:n.1396-11A=
NM_001350627.2:c.871-11A= NP_001337556.1:n.871-11A=
NR_146879.2:n.1579-11A=