Canonical Allele Identifier: CA2676747136

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177604478-G-GCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604480_177604482dup , CM000667.2:g.177604480_177604482dup	GRCh38
NC_000005.9:g.177031481_177031483dup , CM000667.1:g.177031481_177031483dup	GRCh37
NC_000005.8:g.176964087_176964089dup	NCBI36
NG_015977.1:g.9363_9365dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.352_354dup MANE Select	ENSP00000029410.5:p.Phe118_Leu119insPhe
ENST00000029410.9:c.352_354dup	ENSP00000029410.5:p.Phe118_Leu119insPhe
ENST00000502420.1:n.331_333dup
ENST00000505433.5:c.352_354dup	ENSP00000425591.1:p.Phe118_Leu119insPhe
ENST00000505468.1:c.10_12dup	ENSP00000420886.1:p.Phe4_Leu5insPhe
ENST00000507061.1:c.169_171dup	ENSP00000423868.1:p.Phe57_Leu58insPhe
ENST00000510761.1:c.10_12dup	ENSP00000423438.1:p.Phe4_Leu5insPhe
NM_007255.2:c.352_354dup	NP_009186.1:p.Phe118_Leu119insPhe
XM_005265805.2:c.10_12dup	XP_005265862.1:p.Phe4_Leu5insPhe
XM_006714816.2:c.-148_-146dup	XP_006714879.1:n.-148_-146dup
XM_011534421.1:c.10_12dup	XP_011532723.1:p.Phe4_Leu5insPhe
XM_006714816.4:c.-148_-146dup	XP_006714879.1:n.-148_-146dup
XM_017008999.2:c.10_12dup	XP_016864488.1:p.Phe4_Leu5insPhe
NM_007255.3:c.352_354dup MANE Select	NP_009186.1:p.Phe118_Leu119insPhe