Canonical Allele Identifier: CA2676747413

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177604654-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604655del , CM000667.2:g.177604655del	GRCh38
NC_000005.9:g.177031656del , CM000667.1:g.177031656del	GRCh37
NC_000005.8:g.176964262del	NCBI36
NG_015977.1:g.9538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.413+114del MANE Select	ENSP00000029410.5:n.413+114del
ENST00000029410.9:c.413+114del	ENSP00000029410.5:n.413+114del
ENST00000502420.1:n.392+114del
ENST00000505433.5:c.413+114del	ENSP00000425591.1:n.413+114del
ENST00000505468.1:c.71+114del	ENSP00000420886.1:n.71+114del
ENST00000507061.1:c.230+114del	ENSP00000423868.1:n.230+114del
ENST00000510761.1:c.71+114del	ENSP00000423438.1:n.71+114del
NM_007255.2:c.413+114del	NP_009186.1:n.413+114del
XM_005265805.2:c.71+114del	XP_005265862.1:n.71+114del
XM_006714816.2:c.-87+114del	XP_006714879.1:n.-87+114del
XM_011534421.1:c.71+114del	XP_011532723.1:n.71+114del
XM_006714816.4:c.-87+114del	XP_006714879.1:n.-87+114del
XM_017008999.2:c.71+114del	XP_016864488.1:n.71+114del
NM_007255.3:c.413+114del MANE Select	NP_009186.1:n.413+114del