Canonical Allele Identifier: CA2022721777

Gene: BCAT1

Linked Data

• dbSNP Id: rs1670516227

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.24828552del , CM000674.2:g.24828552del	GRCh38
NC_000012.11:g.24981486del , CM000674.1:g.24981486del	GRCh37
NC_000012.10:g.24872753del	NCBI36
NG_008170.1:g.125829del
NG_008170.2:g.125829del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261192.12:c.1119+1277del MANE Select	ENSP00000261192.7:n.1119+1277del
ENST00000261192.11:c.1119+1277del	ENSP00000261192.7:n.1119+1277del
ENST00000342945.9:c.936+1277del	ENSP00000339805.5:n.936+1277del
ENST00000538118.5:c.1116+1277del	ENSP00000440817.1:n.1116+1277del
ENST00000539282.5:c.1155+1277del	ENSP00000443459.1:n.1155+1277del
ENST00000539780.5:c.1008+1277del	ENSP00000440827.1:n.1008+1277del
ENST00000543099.1:n.174+1277del
NM_001178091.1:c.1008+1277del	NP_001171562.1:n.1008+1277del
NM_001178092.1:c.936+1277del	NP_001171563.1:n.936+1277del
NM_001178093.1:c.1155+1277del	NP_001171564.1:n.1155+1277del
NM_001178094.1:c.1116+1277del	NP_001171565.1:n.1116+1277del
NM_005504.6:c.1119+1277del	NP_005495.2:n.1119+1277del
XM_011520810.1:c.1155+1277del	XP_011519112.1:n.1155+1277del
XR_931441.1:n.1532-2149del
XR_931442.1:n.1532-2149del
XR_931443.1:n.1439-2149del
XM_017019768.2:c.1221+1277del	XP_016875257.1:n.1221+1277del
XR_001748835.2:n.4171+1277del
XR_001749047.1:n.3978-2149del
XR_001749048.2:n.3978-2149del
XR_001749049.1:n.3885-2149del
NM_005504.7:c.1119+1277del MANE Select	NP_005495.2:n.1119+1277del
NM_001178091.2:c.1008+1277del	NP_001171562.1:n.1008+1277del
NM_001178092.2:c.936+1277del	NP_001171563.1:n.936+1277del
NM_001178093.2:c.1155+1277del	NP_001171564.1:n.1155+1277del
NM_001178094.2:c.1116+1277del	NP_001171565.1:n.1116+1277del