Canonical Allele Identifier: CA6655549

Gene: B4GALNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57628241G>A , CM000674.2:g.57628241G>A	GRCh38
NC_000012.11:g.58022024G>A , CM000674.1:g.58022024G>A	GRCh37
NC_000012.10:g.56308291G>A	NCBI36
NG_033849.1:g.9999C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341156.9:c.1024C>T MANE Select	ENSP00000341562.4:p.Leu342=
ENST00000341156.8:c.1024C>T	ENSP00000341562.4:p.Leu342=
ENST00000418555.6:c.859C>T	ENSP00000401601.2:p.Leu287=
ENST00000547741.1:c.39C>T
ENST00000549391.5:c.805C>T
ENST00000552468.1:n.1125C>T
ENST00000552798.5:c.*287C>T	ENSP00000447076.1:n.*287C>T
ENST00000553142.5:n.1405C>T
NM_001276468.1:c.859C>T	NP_001263397.1:p.Leu287=
NM_001478.4:c.1024C>T	NP_001469.1:p.Leu342=
XM_005268773.3:c.1024C>T	XP_005268830.1:p.Leu342=
XM_011538147.1:c.1042C>T	XP_011536449.1:p.Leu348=
XM_011538148.1:c.1042C>T	XP_011536450.1:p.Leu348=
XM_005268773.5:c.1024C>T	XP_005268830.1:p.Leu342=
XM_011538147.3:c.1042C>T	XP_011536449.1:p.Leu348=
XM_017019140.2:c.1159C>T	XP_016874629.1:p.Leu387=
XM_017019141.1:c.1159C>T	XP_016874630.1:p.Leu387=
XM_017019142.1:c.1024C>T	XP_016874631.1:p.Leu342=
XM_024448928.1:c.1042C>T	XP_024304696.1:p.Leu348=
XM_024448929.1:c.469C>T	XP_024304697.1:p.Leu157=
XR_002957307.1:n.1178C>T
NM_001478.5:c.1024C>T MANE Select	NP_001469.1:p.Leu342=
NM_001276468.2:c.859C>T	NP_001263397.1:p.Leu287=