Canonical Allele Identifier: CA1905675933
Gene: BMS1 HGNC NCBI

Linked Data

dbSNP Id: rs1841747513

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.42798138_42798139del , CM000672.2:g.42798138_42798139del GRCh38
NC_000010.10:g.43293586_43293587del , CM000672.1:g.43293586_43293587del GRCh37
NC_000010.9:g.42613592_42613593del NCBI36
NG_046921.1:g.20633_20634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374518.6:c.2090-330_2090-329del MANE Select ENSP00000363642.4:n.2090-330_2090-329del
ENST00000374518.5:c.2090-330_2090-329del ENSP00000363642.4:n.2090-330_2090-329del
NM_014753.3:c.2090-330_2090-329del NP_055568.3:n.2090-330_2090-329del
XM_005271846.2:c.2090-330_2090-329del XP_005271903.1:n.2090-330_2090-329del
XM_005271847.2:c.1901-330_1901-329del XP_005271904.1:n.1901-330_1901-329del
XM_005271848.2:c.2090-330_2090-329del XP_005271905.1:n.2090-330_2090-329del
XM_005271849.2:c.2090-330_2090-329del XP_005271906.1:n.2090-330_2090-329del
XM_006718081.2:c.2090-330_2090-329del XP_006718144.1:n.2090-330_2090-329del
XM_011540402.1:c.2090-330_2090-329del XP_011538704.1:n.2090-330_2090-329del
XM_011540403.1:c.857-330_857-329del XP_011538705.1:n.857-330_857-329del
XR_246522.1:n.2179-330_2179-329del
XR_428728.2:n.2179-330_2179-329del
XM_005271846.3:c.2090-330_2090-329del XP_005271903.1:n.2090-330_2090-329del
XM_005271848.3:c.2090-330_2090-329del XP_005271905.1:n.2090-330_2090-329del
XM_011540402.2:c.2090-330_2090-329del XP_011538704.1:n.2090-330_2090-329del
XM_011540403.2:c.857-330_857-329del XP_011538705.1:n.857-330_857-329del
XR_001747266.1:n.2179-330_2179-329del
XR_002957049.1:n.2179-330_2179-329del
NM_014753.4:c.2090-330_2090-329del MANE Select NP_055568.3:n.2090-330_2090-329del