Canonical Allele Identifier: CA2323503493

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657041C= , CM000681.2:g.12657041C=	GRCh38
NC_000019.9:g.12767855C= , CM000681.1:g.12767855C=	GRCh37
NC_000019.8:g.12628855C=	NCBI36
NG_008318.1:g.14737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1435G= MANE Select	ENSP00000395473.2:p.Ala479=
ENST00000221363.8:c.1432G=	ENSP00000221363.4:p.Ala478=
ENST00000433513.5:n.41G=
ENST00000456935.6:c.1435G=	ENSP00000395473.2:p.Ala479=
ENST00000466794.5:n.1334G=
ENST00000495617.1:n.611G=
ENST00000593686.1:c.45G=
ENST00000595880.5:n.32G=
NM_000528.3:c.1435G=	NP_000519.2:p.Ala479=
NM_001173498.1:c.1432G=	NP_001166969.1:p.Ala478=
XM_005259913.1:c.1438G=	XP_005259970.1:p.Ala480=
XM_011528017.1:c.334G=	XP_011526319.1:p.Ala112=
XM_005259913.2:c.1438G=	XP_005259970.1:p.Ala480=
XM_024451518.1:c.334G=	XP_024307286.1:p.Ala112=
NM_000528.4:c.1435G= MANE Select	NP_000519.2:p.Ala479=
NM_001173498.2:c.1432G=	NP_001166969.1:p.Ala478=