Canonical Allele Identifier: CA2832548338

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604556dup , CM000667.2:g.177604556dup	GRCh38
NC_000005.9:g.177031557dup , CM000667.1:g.177031557dup	GRCh37
NC_000005.8:g.176964163dup	NCBI36
NG_015977.1:g.9439dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.413+15dup MANE Select	ENSP00000029410.5:n.413+15dup
ENST00000029410.9:c.413+15dup	ENSP00000029410.5:n.413+15dup
ENST00000502420.1:n.392+15dup
ENST00000505433.5:c.413+15dup	ENSP00000425591.1:n.413+15dup
ENST00000505468.1:c.71+15dup	ENSP00000420886.1:n.71+15dup
ENST00000507061.1:c.230+15dup	ENSP00000423868.1:n.230+15dup
ENST00000510761.1:c.71+15dup	ENSP00000423438.1:n.71+15dup
NM_007255.2:c.413+15dup	NP_009186.1:n.413+15dup
XM_005265805.2:c.71+15dup	XP_005265862.1:n.71+15dup
XM_006714816.2:c.-87+15dup	XP_006714879.1:n.-87+15dup
XM_011534421.1:c.71+15dup	XP_011532723.1:n.71+15dup
XM_006714816.4:c.-87+15dup	XP_006714879.1:n.-87+15dup
XM_017008999.2:c.71+15dup	XP_016864488.1:n.71+15dup
NM_007255.3:c.413+15dup MANE Select	NP_009186.1:n.413+15dup