Canonical Allele Identifier: CA1844936106

Gene: B4GALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.33122516_33122519delinsAAAT , CM000671.2:g.33122516_33122519delinsAAAT	GRCh38
NC_000009.11:g.33122514_33122517delinsAAAT , CM000671.1:g.33122514_33122517delinsAAAT	GRCh37
NC_000009.10:g.33112514_33112517delinsAAAT	NCBI36
NG_008919.1:g.49840_49843delinsATTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000379731.5:c.649-1913_649-1910delinsATTT MANE Select	ENSP00000369055.4:n.649-1913_649-1910delinsATTT
ENST00000379731.4:c.649-1913_649-1910delinsATTT	ENSP00000369055.4:n.649-1913_649-1910delinsATTT
ENST00000535206.5:c.648+12670_648+12673delinsATTT	ENSP00000440341.1:n.648+12670_648+12673delinsATTT
NM_001497.3:c.649-1913_649-1910delinsATTT	NP_001488.2:n.649-1913_649-1910delinsATTT
XM_005251440.3:c.649-1913_649-1910delinsATTT	XP_005251497.1:n.649-1913_649-1910delinsATTT
XM_005251440.5:c.649-1913_649-1910delinsATTT	XP_005251497.1:n.649-1913_649-1910delinsATTT
NM_001378495.1:c.610-1913_610-1910delinsATTT	NP_001365424.1:n.610-1913_610-1910delinsATTT
NM_001378496.1:c.649-1913_649-1910delinsATTT	NP_001365425.1:n.649-1913_649-1910delinsATTT
NM_001378497.1:c.648+12670_648+12673delinsATTT	NP_001365426.1:n.648+12670_648+12673delinsATTT
NM_001497.4:c.649-1913_649-1910delinsATTT MANE Select	NP_001488.2:n.649-1913_649-1910delinsATTT