Canonical Allele Identifier: CA1683199337

Gene: BRAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2539837T= , CM000669.2:g.2539837T=	GRCh38
NC_000007.13:g.2579471T= , CM000669.1:g.2579471T=	GRCh37
NC_000007.12:g.2545997T=	NCBI36
NG_032167.1:g.20922A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1447A= MANE Select	ENSP00000339637.4:p.Lys483=
ENST00000340611.8:c.1447A=	ENSP00000339637.4:p.Lys483=
ENST00000467558.5:n.2819A=
ENST00000469750.5:n.4019A=
ENST00000473879.1:n.163A=
ENST00000493232.5:n.4183A=
NM_152743.3:c.1447A=	NP_689956.2:p.Lys483=
XM_005249643.3:c.1447A=	XP_005249700.1:p.Lys483=
XM_011515177.1:c.1531A=	XP_011513479.1:p.Lys511=
XM_011515178.1:c.1531A=	XP_011513480.1:p.Lys511=
XM_011515179.1:c.1528A=	XP_011513481.1:p.Lys510=
XM_011515180.1:c.1501A=	XP_011513482.1:p.Lys501=
XM_011515181.1:c.1531A=	XP_011513483.1:p.Lys511=
XM_011515182.1:c.1531A=	XP_011513484.1:p.Lys511=
XM_011515183.1:c.1006A=	XP_011513485.1:p.Lys336=
XM_011515184.1:c.1006A=	XP_011513486.1:p.Lys336=
XM_011515185.1:c.1447A=	XP_011513487.1:p.Lys483=
XM_011515186.1:c.1531A=	XP_011513488.1:p.Lys511=
XM_011515187.1:c.103A=	XP_011513489.1:p.Lys35=
NM_001350626.1:c.1447A=	NP_001337555.1:p.Lys483=
NM_001350627.1:c.922A=	NP_001337556.1:p.Lys308=
NR_146879.1:n.1864A=
XM_011515177.2:c.1531A=	XP_011513479.1:p.Lys511=
XM_011515179.2:c.1528A=	XP_011513481.1:p.Lys510=
XM_011515181.2:c.1531A=	XP_011513483.1:p.Lys511=
XM_011515182.2:c.1531A=	XP_011513484.1:p.Lys511=
XM_011515184.3:c.1006A=	XP_011513486.1:p.Lys336=
XM_011515186.2:c.1531A=	XP_011513488.1:p.Lys511=
XM_017011833.1:c.1444A=	XP_016867322.1:p.Lys482=
XM_017011834.1:c.1444A=	XP_016867323.1:p.Lys482=
XM_017011836.2:c.1447A=	XP_016867325.1:p.Lys483=
XM_024446682.1:c.103A=	XP_024302450.1:p.Lys35=
NM_152743.4:c.1447A= MANE Select	NP_689956.2:p.Lys483=
NM_001350626.2:c.1447A=	NP_001337555.1:p.Lys483=
NM_001350627.2:c.922A=	NP_001337556.1:p.Lys308=
NR_146879.2:n.1630A=