Canonical Allele Identifier: CA1683198553

Gene: BRAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2538581C= , CM000669.2:g.2538581C=	GRCh38
NC_000007.13:g.2578215C= , CM000669.1:g.2578215C=	GRCh37
NC_000007.12:g.2544741C=	NCBI36
NG_032167.1:g.22178G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340611.9:c.1954G= MANE Select	ENSP00000339637.4:p.Ala652=
ENST00000340611.8:c.1954G=	ENSP00000339637.4:p.Ala652=
ENST00000467558.5:n.3740G=
ENST00000469750.5:n.4526G=
ENST00000473879.1:n.497G=
ENST00000493232.5:n.4660G=
NM_152743.3:c.1954G=	NP_689956.2:p.Ala652=
XM_005249643.3:c.2134G=	XP_005249700.1:p.Ala712=
XM_011515177.1:c.2218G=	XP_011513479.1:p.Ala740=
XM_011515178.1:c.2218G=	XP_011513480.1:p.Ala740=
XM_011515179.1:c.2215G=	XP_011513481.1:p.Ala739=
XM_011515180.1:c.2188G=	XP_011513482.1:p.Ala730=
XM_011515181.1:c.2038G=	XP_011513483.1:p.Ala680=
XM_011515182.1:c.2218G=	XP_011513484.1:p.Ala740=
XM_011515183.1:c.1693G=	XP_011513485.1:p.Ala565=
XM_011515184.1:c.1693G=	XP_011513486.1:p.Ala565=
XM_011515185.1:c.1954G=	XP_011513487.1:p.Ala652=
XM_011515187.1:c.790G=	XP_011513489.1:p.Ala264=
NM_001350626.1:c.2134G=	NP_001337555.1:p.Ala712=
NM_001350627.1:c.1429G=	NP_001337556.1:p.Ala477=
NR_146879.1:n.2371G=
XM_011515177.2:c.2218G=	XP_011513479.1:p.Ala740=
XM_011515179.2:c.2215G=	XP_011513481.1:p.Ala739=
XM_011515181.2:c.2038G=	XP_011513483.1:p.Ala680=
XM_011515182.2:c.2218G=	XP_011513484.1:p.Ala740=
XM_011515184.3:c.1693G=	XP_011513486.1:p.Ala565=
XM_011515186.2:c.*101G=	XP_011513488.1:n.*101G=
XM_017011833.1:c.2131G=	XP_016867322.1:p.Ala711=
XM_017011834.1:c.1951G=	XP_016867323.1:p.Ala651=
XM_017011836.2:c.*101G=	XP_016867325.1:n.*101G=
XM_024446682.1:c.790G=	XP_024302450.1:p.Ala264=
NM_152743.4:c.1954G= MANE Select	NP_689956.2:p.Ala652=
NM_001350626.2:c.2134G=	NP_001337555.1:p.Ala712=
NM_001350627.2:c.1429G=	NP_001337556.1:p.Ala477=
NR_146879.2:n.2137G=