Canonical Allele Identifier: CA2343355762
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308531_55308532delinsCA , CM000681.2:g.55308531_55308532delinsCA GRCh38
NC_000019.9:g.55819899_55819900delinsCA , CM000681.1:g.55819899_55819900delinsCA GRCh37
NC_000019.8:g.60511711_60511712delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-108_2090-107delinsCA MANE Select ENSP00000310649.1:n.2090-108_2090-107delinsCA
ENST00000309383.5:c.2090-108_2090-107delinsCA ENSP00000310649.1:n.2090-108_2090-107delinsCA
ENST00000326848.7:c.1175-108_1175-107delinsCA ENSP00000320853.7:n.1175-108_1175-107delinsCA
ENST00000590333.5:c.2138-108_2138-107delinsCA ENSP00000468190.1:n.2138-108_2138-107delinsCA
NM_032430.1:c.2090-108_2090-107delinsCA NP_115806.1:n.2090-108_2090-107delinsCA
XM_005259327.2:c.1820-108_1820-107delinsCA XP_005259384.1:n.1820-108_1820-107delinsCA
XM_011527395.1:c.1847-108_1847-107delinsCA XP_011525697.1:n.1847-108_1847-107delinsCA
XR_430213.2:n.2073-108_2073-107delinsCA
XM_005259327.3:c.1820-108_1820-107delinsCA XP_005259384.1:n.1820-108_1820-107delinsCA
XM_011527395.2:c.1562-108_1562-107delinsCA XP_011525697.2:n.1562-108_1562-107delinsCA
XM_024451739.1:c.1865-108_1865-107delinsCA XP_024307507.1:n.1865-108_1865-107delinsCA
XR_430213.4:n.2371-108_2371-107delinsCA
NM_032430.2:c.2090-108_2090-107delinsCA MANE Select NP_115806.1:n.2090-108_2090-107delinsCA