Canonical Allele Identifier: CA387720683

Gene: B3GLCT

Linked Data

• MyVariant Identifiers: chr13:g.31843368A>C (hg19) ; chr13:g.31269231A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31269231A>C , CM000675.2:g.31269231A>C	GRCh38
NC_000013.10:g.31843368A>C , CM000675.1:g.31843368A>C	GRCh37
NC_000013.9:g.30741368A>C	NCBI36
NG_011732.1:g.74257A>C
NG_011732.2:g.74257A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.614A>C MANE Select	ENSP00000343002.4:p.Lys205Thr
ENST00000343307.4:c.614A>C	ENSP00000343002.4:p.Lys205Thr
ENST00000461652.2:n.229A>C
NM_194318.3:c.614A>C	NP_919299.3:p.Lys205Thr
XM_006719768.2:c.557A>C	XP_006719831.1:p.Lys186Thr
XM_011534936.1:c.614A>C	XP_011533238.1:p.Lys205Thr
XM_011534937.1:c.614A>C	XP_011533239.1:p.Lys205Thr
XM_011534938.1:c.467A>C	XP_011533240.1:p.Lys156Thr
XR_941500.1:n.713A>C
XR_941501.1:n.713A>C
XM_006719768.3:c.557A>C	XP_006719831.1:p.Lys186Thr
XM_011534938.2:c.467A>C	XP_011533240.1:p.Lys156Thr
XM_017020395.1:c.467A>C	XP_016875884.1:p.Lys156Thr
NM_194318.4:c.614A>C MANE Select	NP_919299.3:p.Lys205Thr