Canonical Allele Identifier: CA2082357758

Gene: B3GLCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317572C= , CM000675.2:g.31317572C=	GRCh38
NC_000013.10:g.31891709C= , CM000675.1:g.31891709C=	GRCh37
NC_000013.9:g.30789709C=	NCBI36
NG_011732.1:g.122598C=
NG_011732.2:g.122598C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.1071C= MANE Select	ENSP00000343002.4:p.Ser357=
ENST00000343307.4:c.1071C=	ENSP00000343002.4:p.Ser357=
NM_194318.3:c.1071C=	NP_919299.3:p.Ser357=
XM_006719768.2:c.1014C=	XP_006719831.1:p.Ser338=
XM_011534936.1:c.1065-6179C=	XP_011533238.1:n.1065-6179C=
XM_011534937.1:c.951C=	XP_011533239.1:p.Ser317=
XM_011534938.1:c.924C=	XP_011533240.1:p.Ser308=
XR_941500.1:n.1256C=
XR_941501.1:n.1136C=
XM_006719768.3:c.1014C=	XP_006719831.1:p.Ser338=
XM_011534938.2:c.924C=	XP_011533240.1:p.Ser308=
XM_017020395.1:c.924C=	XP_016875884.1:p.Ser308=
NM_194318.4:c.1071C= MANE Select	NP_919299.3:p.Ser357=