Canonical Allele Identifier: CA2022721900
Gene: BCAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.24828687_24828688delinsAT , CM000674.2:g.24828687_24828688delinsAT GRCh38
NC_000012.11:g.24981621_24981622delinsAT , CM000674.1:g.24981621_24981622delinsAT GRCh37
NC_000012.10:g.24872888_24872889delinsAT NCBI36
NG_008170.1:g.125687_125688delinsAT
NG_008170.2:g.125687_125688delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261192.12:c.1119+1135_1119+1136delinsAT MANE Select ENSP00000261192.7:n.1119+1135_1119+1136delinsAT
ENST00000261192.11:c.1119+1135_1119+1136delinsAT ENSP00000261192.7:n.1119+1135_1119+1136delinsAT
ENST00000342945.9:c.936+1135_936+1136delinsAT ENSP00000339805.5:n.936+1135_936+1136delinsAT
ENST00000538118.5:c.1116+1135_1116+1136delinsAT ENSP00000440817.1:n.1116+1135_1116+1136delinsAT
ENST00000539282.5:c.1155+1135_1155+1136delinsAT ENSP00000443459.1:n.1155+1135_1155+1136delinsAT
ENST00000539780.5:c.1008+1135_1008+1136delinsAT ENSP00000440827.1:n.1008+1135_1008+1136delinsAT
ENST00000543099.1:n.174+1135_174+1136delinsAT
NM_001178091.1:c.1008+1135_1008+1136delinsAT NP_001171562.1:n.1008+1135_1008+1136delinsAT
NM_001178092.1:c.936+1135_936+1136delinsAT NP_001171563.1:n.936+1135_936+1136delinsAT
NM_001178093.1:c.1155+1135_1155+1136delinsAT NP_001171564.1:n.1155+1135_1155+1136delinsAT
NM_001178094.1:c.1116+1135_1116+1136delinsAT NP_001171565.1:n.1116+1135_1116+1136delinsAT
NM_005504.6:c.1119+1135_1119+1136delinsAT NP_005495.2:n.1119+1135_1119+1136delinsAT
XM_011520810.1:c.1155+1135_1155+1136delinsAT XP_011519112.1:n.1155+1135_1155+1136delinsAT
XR_931441.1:n.1532-2014_1532-2013delinsAT
XR_931442.1:n.1532-2014_1532-2013delinsAT
XR_931443.1:n.1439-2014_1439-2013delinsAT
XM_017019768.2:c.1221+1135_1221+1136delinsAT XP_016875257.1:n.1221+1135_1221+1136delinsAT
XR_001748835.2:n.4171+1135_4171+1136delinsAT
XR_001749047.1:n.3978-2014_3978-2013delinsAT
XR_001749048.2:n.3978-2014_3978-2013delinsAT
XR_001749049.1:n.3885-2014_3885-2013delinsAT
NM_005504.7:c.1119+1135_1119+1136delinsAT MANE Select NP_005495.2:n.1119+1135_1119+1136delinsAT
NM_001178091.2:c.1008+1135_1008+1136delinsAT NP_001171562.1:n.1008+1135_1008+1136delinsAT
NM_001178092.2:c.936+1135_936+1136delinsAT NP_001171563.1:n.936+1135_936+1136delinsAT
NM_001178093.2:c.1155+1135_1155+1136delinsAT NP_001171564.1:n.1155+1135_1155+1136delinsAT
NM_001178094.2:c.1116+1135_1116+1136delinsAT NP_001171565.1:n.1116+1135_1116+1136delinsAT