Canonical Allele Identifier: CA1844936075

Gene: B4GALT1

Linked Data

• dbSNP Id: rs1840035766

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.33122510_33122511insTAAA , CM000671.2:g.33122510_33122511insTAAA	GRCh38
NC_000009.11:g.33122508_33122509insTAAA , CM000671.1:g.33122508_33122509insTAAA	GRCh37
NC_000009.10:g.33112508_33112509insTAAA	NCBI36
NG_008919.1:g.49851_49852insATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379731.5:c.649-1902_649-1901insATTT MANE Select	ENSP00000369055.4:n.649-1902_649-1901insATTT
ENST00000379731.4:c.649-1902_649-1901insATTT	ENSP00000369055.4:n.649-1902_649-1901insATTT
ENST00000535206.5:c.648+12681_648+12682insATTT	ENSP00000440341.1:n.648+12681_648+12682insATTT
NM_001497.3:c.649-1902_649-1901insATTT	NP_001488.2:n.649-1902_649-1901insATTT
XM_005251440.3:c.649-1902_649-1901insATTT	XP_005251497.1:n.649-1902_649-1901insATTT
XM_005251440.5:c.649-1902_649-1901insATTT	XP_005251497.1:n.649-1902_649-1901insATTT
NM_001378495.1:c.610-1902_610-1901insATTT	NP_001365424.1:n.610-1902_610-1901insATTT
NM_001378496.1:c.649-1902_649-1901insATTT	NP_001365425.1:n.649-1902_649-1901insATTT
NM_001378497.1:c.648+12681_648+12682insATTT	NP_001365426.1:n.648+12681_648+12682insATTT
NM_001497.4:c.649-1902_649-1901insATTT MANE Select	NP_001488.2:n.649-1902_649-1901insATTT