Canonical Allele Identifier: CA1884294573
Gene: MAN1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137101088C= , CM000671.2:g.137101088C= GRCh38
NC_000009.11:g.139995540C= , CM000671.1:g.139995540C= GRCh37
NC_000009.10:g.139115361C= NCBI36
NG_031978.1:g.19162C=

Transcript Alleles

HGVS Amino-acid Change
NM_016219.5:c.1000C= MANE Select NP_057303.2:p.Arg334=
ENST00000371589.9:c.1000C= MANE Select ENSP00000360645.4:p.Arg334=
NM_016219.4:c.1000C= NP_057303.2:p.Arg334=
NR_045720.1:n.1073C=
NR_045720.2:n.1015C=
NR_045721.1:n.1204C=
NR_045721.2:n.1146C=
ENST00000371587.8:c.1050C= ENSP00000483132.1:n.1050C=
ENST00000371587.9:c.*702C= ENSP00000483132.2:n.*702C=
ENST00000371589.8:c.1000C= ENSP00000360645.4:p.Arg334=
ENST00000474902.5:n.646C=
ENST00000475449.7:c.814C= ENSP00000448658.2:p.Arg272=
ENST00000535144.5:c.892C= ENSP00000441398.2:p.Arg298=
ENST00000535144.6:c.1000C= ENSP00000441398.3:p.Arg334=
ENST00000542372.2:c.916C= ENSP00000444189.2:p.Arg306=
ENST00000544448.5:c.1000C= ENSP00000444966.2:p.Arg334=
ENST00000544448.6:c.1000C= ENSP00000444966.2:p.Arg334=
ENST00000545539.6:c.*905C= ENSP00000440314.2:n.*905C=
ENST00000682117.1:c.1000C= ENSP00000507328.1:p.Arg334=
ENST00000682210.1:n.2147C=
ENST00000682212.1:c.1000C= ENSP00000508217.1:p.Arg334=
ENST00000682425.1:n.1250C=
ENST00000682881.1:c.1000C= ENSP00000506762.1:p.Arg334=
ENST00000682964.1:n.348C=
ENST00000683135.1:c.1000C= ENSP00000507130.1:p.Arg334=
ENST00000683324.1:c.997C= ENSP00000507373.1:p.Arg333=
ENST00000683355.1:c.1000C= ENSP00000508045.1:p.Arg334=
ENST00000683475.1:c.1000C= ENSP00000507749.1:p.Arg334=
ENST00000683979.1:c.*702C= ENSP00000507362.1:n.*702C=
ENST00000683987.1:c.1000C= ENSP00000507715.1:p.Arg334=
ENST00000684138.1:c.*702C= ENSP00000506755.1:n.*702C=
ENST00000684144.1:c.997C= ENSP00000508213.1:p.Arg333=
ENST00000684229.1:n.1043C=
ENST00000684272.1:c.*905C= ENSP00000506776.1:n.*905C=
ENST00000684297.1:c.1000C= ENSP00000507160.1:p.Arg334=
ENST00000684366.1:c.1000C= ENSP00000507668.1:p.Arg334=
ENST00000684645.1:n.1020C=
ENST00000684759.1:c.1000C= ENSP00000507818.1:p.Arg334=
XM_006716945.2:c.1000C= XP_006717008.1:p.Arg334=
XM_006716945.4:c.1000C= XP_006717008.1:p.Arg334=
XM_017014239.1:c.703C= XP_016869728.1:p.Arg235=
XM_024447403.1:c.1000C= XP_024303171.1:p.Arg334=
XR_001746176.1:n.1190C=