Canonical Allele Identifier: CA6484778

Gene: BCAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.24832804C>T , CM000674.2:g.24832804C>T	GRCh38
NC_000012.11:g.24985738C>T , CM000674.1:g.24985738C>T	GRCh37
NC_000012.10:g.24877005C>T	NCBI36
NG_008170.1:g.121571G>A
NG_008170.2:g.121571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261192.12:c.963G>A MANE Select	ENSP00000261192.7:p.Glu321=
ENST00000261192.11:c.963G>A	ENSP00000261192.7:p.Glu321=
ENST00000342945.9:c.780G>A	ENSP00000339805.5:p.Glu260=
ENST00000538118.5:c.960G>A	ENSP00000440817.1:p.Glu320=
ENST00000539282.5:c.999G>A	ENSP00000443459.1:p.Glu333=
ENST00000539780.5:c.852G>A	ENSP00000440827.1:p.Glu284=
NM_001178091.1:c.852G>A	NP_001171562.1:p.Glu284=
NM_001178092.1:c.780G>A	NP_001171563.1:p.Glu260=
NM_001178093.1:c.999G>A	NP_001171564.1:p.Glu333=
NM_001178094.1:c.960G>A	NP_001171565.1:p.Glu320=
NM_005504.6:c.963G>A	NP_005495.2:p.Glu321=
XM_011520810.1:c.999G>A	XP_011519112.1:p.Glu333=
XR_931441.1:n.1620+2015C>T
XR_931442.1:n.1621-1500C>T
XR_931443.1:n.1527+2015C>T
XM_017019768.2:c.1065G>A	XP_016875257.1:p.Glu355=
XR_001748835.2:n.4015G>A
XR_001749047.1:n.4066+2015C>T
XR_001749048.2:n.4067-1500C>T
NM_005504.7:c.963G>A MANE Select	NP_005495.2:p.Glu321=
NM_001178091.2:c.852G>A	NP_001171562.1:p.Glu284=
NM_001178092.2:c.780G>A	NP_001171563.1:p.Glu260=
NM_001178093.2:c.999G>A	NP_001171564.1:p.Glu333=
NM_001178094.2:c.960G>A	NP_001171565.1:p.Glu320=