Canonical Allele Identifier: CA2769581863

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604308_177604310del , CM000667.2:g.177604308_177604310del	GRCh38
NC_000005.9:g.177031309_177031311del , CM000667.1:g.177031309_177031311del	GRCh37
NC_000005.8:g.176963915_176963917del	NCBI36
NG_015977.1:g.9191_9193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.180_182del MANE Select	ENSP00000029410.5:p.Val61del
ENST00000029410.9:c.180_182del	ENSP00000029410.5:p.Val61del
ENST00000502420.1:n.159_161del
ENST00000505433.5:c.180_182del	ENSP00000425591.1:p.Val61del
ENST00000505468.1:c.-163_-161del	ENSP00000420886.1:n.-163_-161del
ENST00000510761.1:c.-163_-161del	ENSP00000423438.1:n.-163_-161del
NM_007255.2:c.180_182del	NP_009186.1:p.Val61del
XM_005265805.2:c.-163_-161del	XP_005265862.1:n.-163_-161del
XM_006714816.2:c.-320_-318del	XP_006714879.1:n.-320_-318del
XM_011534421.1:c.-163_-161del	XP_011532723.1:n.-163_-161del
XM_006714816.4:c.-320_-318del	XP_006714879.1:n.-320_-318del
XM_017008999.2:c.-163_-161del	XP_016864488.1:n.-163_-161del
NM_007255.3:c.180_182del MANE Select	NP_009186.1:p.Val61del