Canonical Allele Identifier: CA2323507874

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665786G= , CM000681.2:g.12665786G=	GRCh38
NC_000019.9:g.12776600G= , CM000681.1:g.12776600G=	GRCh37
NC_000019.8:g.12637600G=	NCBI36
NG_008318.1:g.5992C=
NG_015814.1:g.3983G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.179C= MANE Select	ENSP00000395473.2:p.Pro60=
ENST00000221363.8:c.179C=	ENSP00000221363.4:p.Pro60=
ENST00000456935.6:c.179C=	ENSP00000395473.2:p.Pro60=
ENST00000466794.5:n.161C=
ENST00000486847.2:c.160-261C=	ENSP00000470174.1:n.160-261C=
ENST00000596512.5:n.201-261C=
ENST00000597961.1:c.170C=	ENSP00000472710.1:p.Pro57=
ENST00000598876.1:c.206C=	ENSP00000470533.1:p.Pro69=
ENST00000600281.1:n.220C=
NM_000528.3:c.179C=	NP_000519.2:p.Pro60=
NM_001173498.1:c.179C=	NP_001166969.1:p.Pro60=
XM_005259913.1:c.179C=	XP_005259970.1:p.Pro60=
XM_005259913.2:c.179C=	XP_005259970.1:p.Pro60=
XM_024451518.1:c.-840C=	XP_024307286.1:n.-840C=
NM_000528.4:c.179C= MANE Select	NP_000519.2:p.Pro60=
NM_001173498.2:c.179C=	NP_001166969.1:p.Pro60=