Canonical Allele Identifier: CA2022721705
Gene: BCAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.24828476_24828477delinsGA , CM000674.2:g.24828476_24828477delinsGA GRCh38
NC_000012.11:g.24981410_24981411delinsGA , CM000674.1:g.24981410_24981411delinsGA GRCh37
NC_000012.10:g.24872677_24872678delinsGA NCBI36
NG_008170.1:g.125898_125899delinsTC
NG_008170.2:g.125898_125899delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261192.12:c.1119+1346_1119+1347delinsTC MANE Select ENSP00000261192.7:n.1119+1346_1119+1347delinsTC
ENST00000261192.11:c.1119+1346_1119+1347delinsTC ENSP00000261192.7:n.1119+1346_1119+1347delinsTC
ENST00000342945.9:c.936+1346_936+1347delinsTC ENSP00000339805.5:n.936+1346_936+1347delinsTC
ENST00000538118.5:c.1116+1346_1116+1347delinsTC ENSP00000440817.1:n.1116+1346_1116+1347delinsTC
ENST00000539282.5:c.1155+1346_1155+1347delinsTC ENSP00000443459.1:n.1155+1346_1155+1347delinsTC
ENST00000539780.5:c.1008+1346_1008+1347delinsTC ENSP00000440827.1:n.1008+1346_1008+1347delinsTC
ENST00000543099.1:n.174+1346_174+1347delinsTC
NM_001178091.1:c.1008+1346_1008+1347delinsTC NP_001171562.1:n.1008+1346_1008+1347delinsTC
NM_001178092.1:c.936+1346_936+1347delinsTC NP_001171563.1:n.936+1346_936+1347delinsTC
NM_001178093.1:c.1155+1346_1155+1347delinsTC NP_001171564.1:n.1155+1346_1155+1347delinsTC
NM_001178094.1:c.1116+1346_1116+1347delinsTC NP_001171565.1:n.1116+1346_1116+1347delinsTC
NM_005504.6:c.1119+1346_1119+1347delinsTC NP_005495.2:n.1119+1346_1119+1347delinsTC
XM_011520810.1:c.1155+1346_1155+1347delinsTC XP_011519112.1:n.1155+1346_1155+1347delinsTC
XR_931441.1:n.1532-2225_1532-2224delinsGA
XR_931442.1:n.1532-2225_1532-2224delinsGA
XR_931443.1:n.1439-2225_1439-2224delinsGA
XM_017019768.2:c.1221+1346_1221+1347delinsTC XP_016875257.1:n.1221+1346_1221+1347delinsTC
XR_001748835.2:n.4171+1346_4171+1347delinsTC
XR_001749047.1:n.3978-2225_3978-2224delinsGA
XR_001749048.2:n.3978-2225_3978-2224delinsGA
XR_001749049.1:n.3885-2225_3885-2224delinsGA
NM_005504.7:c.1119+1346_1119+1347delinsTC MANE Select NP_005495.2:n.1119+1346_1119+1347delinsTC
NM_001178091.2:c.1008+1346_1008+1347delinsTC NP_001171562.1:n.1008+1346_1008+1347delinsTC
NM_001178092.2:c.936+1346_936+1347delinsTC NP_001171563.1:n.936+1346_936+1347delinsTC
NM_001178093.2:c.1155+1346_1155+1347delinsTC NP_001171564.1:n.1155+1346_1155+1347delinsTC
NM_001178094.2:c.1116+1346_1116+1347delinsTC NP_001171565.1:n.1116+1346_1116+1347delinsTC