Canonical Allele Identifier: CA1905675859
Gene: BMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.42798080A= , CM000672.2:g.42798080A= GRCh38
NC_000010.10:g.43293528A= , CM000672.1:g.43293528A= GRCh37
NC_000010.9:g.42613534A= NCBI36
NG_046921.1:g.20575A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374518.6:c.2090-388A= MANE Select ENSP00000363642.4:n.2090-388A=
ENST00000374518.5:c.2090-388A= ENSP00000363642.4:n.2090-388A=
NM_014753.3:c.2090-388A= NP_055568.3:n.2090-388A=
XM_005271846.2:c.2090-388A= XP_005271903.1:n.2090-388A=
XM_005271847.2:c.1901-388A= XP_005271904.1:n.1901-388A=
XM_005271848.2:c.2090-388A= XP_005271905.1:n.2090-388A=
XM_005271849.2:c.2090-388A= XP_005271906.1:n.2090-388A=
XM_006718081.2:c.2090-388A= XP_006718144.1:n.2090-388A=
XM_011540402.1:c.2090-388A= XP_011538704.1:n.2090-388A=
XM_011540403.1:c.857-388A= XP_011538705.1:n.857-388A=
XR_246522.1:n.2179-388A=
XR_428728.2:n.2179-388A=
XM_005271846.3:c.2090-388A= XP_005271903.1:n.2090-388A=
XM_005271848.3:c.2090-388A= XP_005271905.1:n.2090-388A=
XM_011540402.2:c.2090-388A= XP_011538704.1:n.2090-388A=
XM_011540403.2:c.857-388A= XP_011538705.1:n.857-388A=
XR_001747266.1:n.2179-388A=
XR_002957049.1:n.2179-388A=
NM_014753.4:c.2090-388A= MANE Select NP_055568.3:n.2090-388A=