Canonical Allele Identifier: CA1844935664
Gene: B4GALT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33122261G= , CM000671.2:g.33122261G= GRCh38
NC_000009.11:g.33122259G= , CM000671.1:g.33122259G= GRCh37
NC_000009.10:g.33112259G= NCBI36
NG_008919.1:g.50098C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379731.5:c.649-1655C= MANE Select ENSP00000369055.4:n.649-1655C=
ENST00000379731.4:c.649-1655C= ENSP00000369055.4:n.649-1655C=
ENST00000535206.5:c.648+12928C= ENSP00000440341.1:n.648+12928C=
NM_001497.3:c.649-1655C= NP_001488.2:n.649-1655C=
XM_005251440.3:c.649-1655C= XP_005251497.1:n.649-1655C=
XM_005251440.5:c.649-1655C= XP_005251497.1:n.649-1655C=
NM_001378495.1:c.610-1655C= NP_001365424.1:n.610-1655C=
NM_001378496.1:c.649-1655C= NP_001365425.1:n.649-1655C=
NM_001378497.1:c.648+12928C= NP_001365426.1:n.648+12928C=
NM_001497.4:c.649-1655C= MANE Select NP_001488.2:n.649-1655C=
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