Canonical Allele Identifier: CA2594899382
Gene: B4GALT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33122513_33122514insTAA , CM000671.2:g.33122513_33122514insTAA GRCh38
NC_000009.11:g.33122511_33122512insTAA , CM000671.1:g.33122511_33122512insTAA GRCh37
NC_000009.10:g.33112511_33112512insTAA NCBI36
NG_008919.1:g.49847_49848insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000379731.5:c.649-1906_649-1905insATT MANE Select ENSP00000369055.4:n.649-1906_649-1905insATT
ENST00000379731.4:c.649-1906_649-1905insATT ENSP00000369055.4:n.649-1906_649-1905insATT
ENST00000535206.5:c.648+12677_648+12678insATT ENSP00000440341.1:n.648+12677_648+12678insATT
NM_001497.3:c.649-1906_649-1905insATT NP_001488.2:n.649-1906_649-1905insATT
XM_005251440.3:c.649-1906_649-1905insATT XP_005251497.1:n.649-1906_649-1905insATT
XM_005251440.5:c.649-1906_649-1905insATT XP_005251497.1:n.649-1906_649-1905insATT
NM_001378495.1:c.610-1906_610-1905insATT NP_001365424.1:n.610-1906_610-1905insATT
NM_001378496.1:c.649-1906_649-1905insATT NP_001365425.1:n.649-1906_649-1905insATT
NM_001378497.1:c.648+12677_648+12678insATT NP_001365426.1:n.648+12677_648+12678insATT
NM_001497.4:c.649-1906_649-1905insATT MANE Select NP_001488.2:n.649-1906_649-1905insATT