Canonical Allele Identifier: CA2323504304

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658291C= , CM000681.2:g.12658291C=	GRCh38
NC_000019.9:g.12769105C= , CM000681.1:g.12769105C=	GRCh37
NC_000019.8:g.12630105C=	NCBI36
NG_008318.1:g.13487G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.1163G= MANE Select	ENSP00000395473.2:p.Trp388=
ENST00000221363.8:c.1160G=	ENSP00000221363.4:p.Trp387=
ENST00000456935.6:c.1163G=	ENSP00000395473.2:p.Trp388=
ENST00000465830.1:n.327G=
ENST00000466794.5:n.1062G=
ENST00000495617.1:n.280+440G=
NM_000528.3:c.1163G=	NP_000519.2:p.Trp388=
NM_001173498.1:c.1160G=	NP_001166969.1:p.Trp387=
XM_005259913.1:c.1166G=	XP_005259970.1:p.Trp389=
XM_011528017.1:c.62G=	XP_011526319.1:p.Trp21=
XM_005259913.2:c.1166G=	XP_005259970.1:p.Trp389=
XM_024451518.1:c.62G=	XP_024307286.1:p.Trp21=
NM_000528.4:c.1163G= MANE Select	NP_000519.2:p.Trp388=
NM_001173498.2:c.1160G=	NP_001166969.1:p.Trp387=