Canonical Allele Identifier: CA2538178805
Gene: B4GALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33122275dup , CM000671.2:g.33122275dup GRCh38
NC_000009.11:g.33122273dup , CM000671.1:g.33122273dup GRCh37
NC_000009.10:g.33112273dup NCBI36
NG_008919.1:g.50085dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379731.5:c.649-1668dup MANE Select ENSP00000369055.4:n.649-1668dup
ENST00000379731.4:c.649-1668dup ENSP00000369055.4:n.649-1668dup
ENST00000535206.5:c.648+12915dup ENSP00000440341.1:n.648+12915dup
NM_001497.3:c.649-1668dup NP_001488.2:n.649-1668dup
XM_005251440.3:c.649-1668dup XP_005251497.1:n.649-1668dup
XM_005251440.5:c.649-1668dup XP_005251497.1:n.649-1668dup
NM_001378495.1:c.610-1668dup NP_001365424.1:n.610-1668dup
NM_001378496.1:c.649-1668dup NP_001365425.1:n.649-1668dup
NM_001378497.1:c.648+12915dup NP_001365426.1:n.648+12915dup
NM_001497.4:c.649-1668dup MANE Select NP_001488.2:n.649-1668dup