Canonical Allele Identifier: CA5358755

Gene: MAN1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137099650G>A , CM000671.2:g.137099650G>A	GRCh38
NC_000009.11:g.139994102G>A , CM000671.1:g.139994102G>A	GRCh37
NC_000009.10:g.139113923G>A	NCBI36
NG_031978.1:g.17724G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016219.5:c.731-46G>A MANE Select	NP_057303.2:n.731-46G>A
ENST00000371589.9:c.731-46G>A MANE Select	ENSP00000360645.4:n.731-46G>A
NM_016219.4:c.731-46G>A	NP_057303.2:n.731-46G>A
NR_045720.1:n.804-46G>A
NR_045720.2:n.746-46G>A
NR_045721.1:n.935-46G>A
NR_045721.2:n.877-46G>A
ENST00000371587.8:c.781-46G>A	ENSP00000483132.1:n.781-46G>A
ENST00000371587.9:c.*433-46G>A	ENSP00000483132.2:n.*433-46G>A
ENST00000371589.8:c.731-46G>A	ENSP00000360645.4:n.731-46G>A
ENST00000474902.5:n.377-46G>A
ENST00000475449.7:c.731-1355G>A	ENSP00000448658.2:n.731-1355G>A
ENST00000535144.5:c.623-46G>A	ENSP00000441398.2:n.623-46G>A
ENST00000535144.6:c.731-46G>A	ENSP00000441398.3:n.731-46G>A
ENST00000542372.2:c.647-46G>A	ENSP00000444189.2:n.647-46G>A
ENST00000544448.5:c.731-46G>A	ENSP00000444966.2:n.731-46G>A
ENST00000544448.6:c.731-46G>A	ENSP00000444966.2:n.731-46G>A
ENST00000545539.6:c.*636-46G>A	ENSP00000440314.2:n.*636-46G>A
ENST00000682117.1:c.731-46G>A	ENSP00000507328.1:n.731-46G>A
ENST00000682210.1:n.755-46G>A
ENST00000682212.1:c.731-46G>A	ENSP00000508217.1:n.731-46G>A
ENST00000682425.1:n.981-46G>A
ENST00000682881.1:c.731-46G>A	ENSP00000506762.1:n.731-46G>A
ENST00000682964.1:n.79-46G>A
ENST00000683113.1:n.364-46G>A
ENST00000683135.1:c.731-46G>A	ENSP00000507130.1:n.731-46G>A
ENST00000683324.1:c.728-46G>A	ENSP00000507373.1:n.728-46G>A
ENST00000683355.1:c.731-46G>A	ENSP00000508045.1:n.731-46G>A
ENST00000683475.1:c.731-46G>A	ENSP00000507749.1:n.731-46G>A
ENST00000683979.1:c.*433-46G>A	ENSP00000507362.1:n.*433-46G>A
ENST00000683987.1:c.731-46G>A	ENSP00000507715.1:n.731-46G>A
ENST00000684138.1:c.*433-46G>A	ENSP00000506755.1:n.*433-46G>A
ENST00000684144.1:c.728-46G>A	ENSP00000508213.1:n.728-46G>A
ENST00000684229.1:n.774-46G>A
ENST00000684272.1:c.*636-46G>A	ENSP00000506776.1:n.*636-46G>A
ENST00000684297.1:c.731-46G>A	ENSP00000507160.1:n.731-46G>A
ENST00000684366.1:c.731-46G>A	ENSP00000507668.1:n.731-46G>A
ENST00000684645.1:n.751-46G>A
ENST00000684759.1:c.731-46G>A	ENSP00000507818.1:n.731-46G>A
XM_006716945.2:c.731-46G>A	XP_006717008.1:n.731-46G>A
XM_006716945.4:c.731-46G>A	XP_006717008.1:n.731-46G>A
XM_017014239.1:c.434-46G>A	XP_016869728.1:n.434-46G>A
XM_024447403.1:c.731-46G>A	XP_024303171.1:n.731-46G>A
XR_001746176.1:n.921-46G>A