Canonical Allele Identifier: CA2578500160

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604303dup , CM000667.2:g.177604303dup	GRCh38
NC_000005.9:g.177031304dup , CM000667.1:g.177031304dup	GRCh37
NC_000005.8:g.176963910dup	NCBI36
NG_015977.1:g.9186dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.175dup MANE Select	ENSP00000029410.5:p.Arg59ProfsTer24
ENST00000029410.9:c.175dup	ENSP00000029410.5:p.Arg59ProfsTer24
ENST00000502420.1:n.154dup
ENST00000505433.5:c.175dup	ENSP00000425591.1:p.Arg59ProfsTer24
ENST00000505468.1:c.-168dup	ENSP00000420886.1:n.-168dup
ENST00000510761.1:c.-168dup	ENSP00000423438.1:n.-168dup
NM_007255.2:c.175dup	NP_009186.1:p.Arg59ProfsTer24
XM_005265805.2:c.-168dup	XP_005265862.1:n.-168dup
XM_006714816.2:c.-325dup	XP_006714879.1:n.-325dup
XM_011534421.1:c.-168dup	XP_011532723.1:n.-168dup
XM_006714816.4:c.-325dup	XP_006714879.1:n.-325dup
XM_017008999.2:c.-168dup	XP_016864488.1:n.-168dup
NM_007255.3:c.175dup MANE Select	NP_009186.1:p.Arg59ProfsTer24