Canonical Allele Identifier: CA385493892

Gene: B4GALNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57627653C>T , CM000674.2:g.57627653C>T	GRCh38
NC_000012.11:g.58021436C>T , CM000674.1:g.58021436C>T	GRCh37
NC_000012.10:g.56307703C>T	NCBI36
NG_033849.1:g.10587G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001478.5:c.1349G>A MANE Select	NP_001469.1:p.Gly450Asp
ENST00000341156.9:c.1349G>A MANE Select	ENSP00000341562.4:p.Gly450Asp
NM_001276468.1:c.1184G>A	NP_001263397.1:p.Gly395Asp
NM_001276468.2:c.1184G>A	NP_001263397.1:p.Gly395Asp
NM_001478.4:c.1349G>A	NP_001469.1:p.Gly450Asp
ENST00000341156.8:c.1349G>A	ENSP00000341562.4:p.Gly450Asp
ENST00000418555.6:c.1184G>A	ENSP00000401601.2:p.Gly395Asp
ENST00000547741.1:c.397G>A
ENST00000552468.1:n.1713G>A
ENST00000552798.5:c.*612G>A	ENSP00000447076.1:n.*612G>A
ENST00000553142.5:n.1993G>A
XM_005268773.3:c.1382G>A	XP_005268830.1:p.Gly461Asp
XM_005268773.5:c.1382G>A	XP_005268830.1:p.Gly461Asp
XM_011538147.1:c.1400G>A	XP_011536449.1:p.Gly467Asp
XM_011538147.3:c.1400G>A	XP_011536449.1:p.Gly467Asp
XM_011538148.1:c.1367G>A	XP_011536450.1:p.Gly456Asp
XM_017019140.2:c.1484G>A	XP_016874629.1:p.Gly495Asp
XM_017019141.1:c.1484G>A	XP_016874630.1:p.Gly495Asp
XM_017019142.1:c.1349G>A	XP_016874631.1:p.Gly450Asp
XM_024448928.1:c.1367G>A	XP_024304696.1:p.Gly456Asp
XM_024448929.1:c.827G>A	XP_024304697.1:p.Gly276Asp
XR_002957307.1:n.1766G>A