Canonical Allele Identifier: CA1683200738

Gene: BRAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2542080_2542081delinsAC , CM000669.2:g.2542080_2542081delinsAC	GRCh38
NC_000007.13:g.2581714_2581715delinsAC , CM000669.1:g.2581714_2581715delinsAC	GRCh37
NC_000007.12:g.2548240_2548241delinsAC	NCBI36
NG_032167.1:g.18678_18679delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000340611.9:c.1015+39_1015+40delinsGT MANE Select	ENSP00000339637.4:n.1015+39_1015+40delins...
ENST00000340611.8:c.1015+39_1015+40delinsGT	ENSP00000339637.4:n.1015+39_1015+40delins...
ENST00000467558.5:n.1297+39_1297+40delinsGT
ENST00000469750.5:n.2497+39_2497+40delinsGT
ENST00000493232.5:n.2172_2173delinsGT
NM_152743.3:c.1015+39_1015+40delinsGT	NP_689956.2:n.1015+39_1015+40delinsGT
XM_005249643.3:c.1015+39_1015+40delinsGT	XP_005249700.1:n.1015+39_1015+40delinsGT
XM_011515177.1:c.1015+39_1015+40delinsGT	XP_011513479.1:n.1015+39_1015+40delinsGT
XM_011515178.1:c.1015+39_1015+40delinsGT	XP_011513480.1:n.1015+39_1015+40delinsGT
XM_011515179.1:c.1012+39_1012+40delinsGT	XP_011513481.1:n.1012+39_1012+40delinsGT
XM_011515180.1:c.985+39_985+40delinsGT	XP_011513482.1:n.985+39_985+40delinsGT
XM_011515181.1:c.1015+39_1015+40delinsGT	XP_011513483.1:n.1015+39_1015+40delinsGT
XM_011515182.1:c.1015+39_1015+40delinsGT	XP_011513484.1:n.1015+39_1015+40delinsGT
XM_011515183.1:c.490+39_490+40delinsGT	XP_011513485.1:n.490+39_490+40delinsGT
XM_011515184.1:c.490+39_490+40delinsGT	XP_011513486.1:n.490+39_490+40delinsGT
XM_011515185.1:c.1015+39_1015+40delinsGT	XP_011513487.1:n.1015+39_1015+40delinsGT
XM_011515186.1:c.1015+39_1015+40delinsGT	XP_011513488.1:n.1015+39_1015+40delinsGT
NM_001350626.1:c.1015+39_1015+40delinsGT	NP_001337555.1:n.1015+39_1015+40delinsGT
NM_001350627.1:c.490+39_490+40delinsGT	NP_001337556.1:n.490+39_490+40delinsGT
NR_146879.1:n.1308+39_1308+40delinsGT
XM_011515177.2:c.1015+39_1015+40delinsGT	XP_011513479.1:n.1015+39_1015+40delinsGT
XM_011515179.2:c.1012+39_1012+40delinsGT	XP_011513481.1:n.1012+39_1012+40delinsGT
XM_011515181.2:c.1015+39_1015+40delinsGT	XP_011513483.1:n.1015+39_1015+40delinsGT
XM_011515182.2:c.1015+39_1015+40delinsGT	XP_011513484.1:n.1015+39_1015+40delinsGT
XM_011515184.3:c.490+39_490+40delinsGT	XP_011513486.1:n.490+39_490+40delinsGT
XM_011515186.2:c.1015+39_1015+40delinsGT	XP_011513488.1:n.1015+39_1015+40delinsGT
XM_017011833.1:c.1012+39_1012+40delinsGT	XP_016867322.1:n.1012+39_1012+40delinsGT
XM_017011834.1:c.1012+39_1012+40delinsGT	XP_016867323.1:n.1012+39_1012+40delinsGT
XM_017011836.2:c.1015+39_1015+40delinsGT	XP_016867325.1:n.1015+39_1015+40delinsGT
NM_152743.4:c.1015+39_1015+40delinsGT MANE Select	NP_689956.2:n.1015+39_1015+40delinsGT
NM_001350626.2:c.1015+39_1015+40delinsGT	NP_001337555.1:n.1015+39_1015+40delinsGT
NM_001350627.2:c.490+39_490+40delinsGT	NP_001337556.1:n.490+39_490+40delinsGT
NR_146879.2:n.1074+39_1074+40delinsGT