Canonical Allele Identifier: CA1123031430
Gene: B4GALT1 HGNC NCBI

Linked Data

dbSNP Id: rs1840036509

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33122537dup , CM000671.2:g.33122537dup GRCh38
NC_000009.11:g.33122535dup , CM000671.1:g.33122535dup GRCh37
NC_000009.10:g.33112535dup NCBI36
NG_008919.1:g.49823dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379731.5:c.649-1930dup MANE Select ENSP00000369055.4:n.649-1930dup
ENST00000379731.4:c.649-1930dup ENSP00000369055.4:n.649-1930dup
ENST00000535206.5:c.648+12653dup ENSP00000440341.1:n.648+12653dup
NM_001497.3:c.649-1930dup NP_001488.2:n.649-1930dup
XM_005251440.3:c.649-1930dup XP_005251497.1:n.649-1930dup
XM_005251440.5:c.649-1930dup XP_005251497.1:n.649-1930dup
NM_001378495.1:c.610-1930dup NP_001365424.1:n.610-1930dup
NM_001378496.1:c.649-1930dup NP_001365425.1:n.649-1930dup
NM_001378497.1:c.648+12653dup NP_001365426.1:n.648+12653dup
NM_001497.4:c.649-1930dup MANE Select NP_001488.2:n.649-1930dup