Canonical Allele Identifier: CA2082357814

Gene: B3GLCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317606G= , CM000675.2:g.31317606G=	GRCh38
NC_000013.10:g.31891743G= , CM000675.1:g.31891743G=	GRCh37
NC_000013.9:g.30789743G=	NCBI36
NG_011732.1:g.122632G=
NG_011732.2:g.122632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.1105G= MANE Select	ENSP00000343002.4:p.Gly369=
ENST00000343307.4:c.1105G=	ENSP00000343002.4:p.Gly369=
NM_194318.3:c.1105G=	NP_919299.3:p.Gly369=
XM_006719768.2:c.1048G=	XP_006719831.1:p.Gly350=
XM_011534936.1:c.1065-6145G=	XP_011533238.1:n.1065-6145G=
XM_011534937.1:c.985G=	XP_011533239.1:p.Gly329=
XM_011534938.1:c.958G=	XP_011533240.1:p.Gly320=
XR_941500.1:n.1290G=
XR_941501.1:n.1170G=
XM_006719768.3:c.1048G=	XP_006719831.1:p.Gly350=
XM_011534938.2:c.958G=	XP_011533240.1:p.Gly320=
XM_017020395.1:c.958G=	XP_016875884.1:p.Gly320=
NM_194318.4:c.1105G= MANE Select	NP_919299.3:p.Gly369=