Canonical Allele Identifier: CA2022721865

Gene: BCAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.24828656_24828658delinsCAT , CM000674.2:g.24828656_24828658delinsCAT	GRCh38
NC_000012.11:g.24981590_24981592delinsCAT , CM000674.1:g.24981590_24981592delinsCAT	GRCh37
NC_000012.10:g.24872857_24872859delinsCAT	NCBI36
NG_008170.1:g.125717_125719delinsATG
NG_008170.2:g.125717_125719delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261192.12:c.1119+1165_1119+1167delinsATG MANE Select	ENSP00000261192.7:n.1119+1165_1119+1167delinsATG
ENST00000261192.11:c.1119+1165_1119+1167delinsATG	ENSP00000261192.7:n.1119+1165_1119+1167delinsATG
ENST00000342945.9:c.936+1165_936+1167delinsATG	ENSP00000339805.5:n.936+1165_936+1167delinsATG
ENST00000538118.5:c.1116+1165_1116+1167delinsATG	ENSP00000440817.1:n.1116+1165_1116+1167delinsATG
ENST00000539282.5:c.1155+1165_1155+1167delinsATG	ENSP00000443459.1:n.1155+1165_1155+1167delinsATG
ENST00000539780.5:c.1008+1165_1008+1167delinsATG	ENSP00000440827.1:n.1008+1165_1008+1167delinsATG
ENST00000543099.1:n.174+1165_174+1167delinsATG
NM_001178091.1:c.1008+1165_1008+1167delinsATG	NP_001171562.1:n.1008+1165_1008+1167delinsATG
NM_001178092.1:c.936+1165_936+1167delinsATG	NP_001171563.1:n.936+1165_936+1167delinsATG
NM_001178093.1:c.1155+1165_1155+1167delinsATG	NP_001171564.1:n.1155+1165_1155+1167delinsATG
NM_001178094.1:c.1116+1165_1116+1167delinsATG	NP_001171565.1:n.1116+1165_1116+1167delinsATG
NM_005504.6:c.1119+1165_1119+1167delinsATG	NP_005495.2:n.1119+1165_1119+1167delinsATG
XM_011520810.1:c.1155+1165_1155+1167delinsATG	XP_011519112.1:n.1155+1165_1155+1167delinsATG
XR_931441.1:n.1532-2045_1532-2043delinsCAT
XR_931442.1:n.1532-2045_1532-2043delinsCAT
XR_931443.1:n.1439-2045_1439-2043delinsCAT
XM_017019768.2:c.1221+1165_1221+1167delinsATG	XP_016875257.1:n.1221+1165_1221+1167delinsATG
XR_001748835.2:n.4171+1165_4171+1167delinsATG
XR_001749047.1:n.3978-2045_3978-2043delinsCAT
XR_001749048.2:n.3978-2045_3978-2043delinsCAT
XR_001749049.1:n.3885-2045_3885-2043delinsCAT
NM_005504.7:c.1119+1165_1119+1167delinsATG MANE Select	NP_005495.2:n.1119+1165_1119+1167delinsATG
NM_001178091.2:c.1008+1165_1008+1167delinsATG	NP_001171562.1:n.1008+1165_1008+1167delinsATG
NM_001178092.2:c.936+1165_936+1167delinsATG	NP_001171563.1:n.936+1165_936+1167delinsATG
NM_001178093.2:c.1155+1165_1155+1167delinsATG	NP_001171564.1:n.1155+1165_1155+1167delinsATG
NM_001178094.2:c.1116+1165_1116+1167delinsATG	NP_001171565.1:n.1116+1165_1116+1167delinsATG