Canonical Allele Identifier: CA2578500111

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604133del , CM000667.2:g.177604133del	GRCh38
NC_000005.9:g.177031134del , CM000667.1:g.177031134del	GRCh37
NC_000005.8:g.176963740del	NCBI36
NG_015977.1:g.9016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.51-46del MANE Select	ENSP00000029410.5:n.51-46del
ENST00000029410.9:c.51-46del	ENSP00000029410.5:n.51-46del
ENST00000502420.1:n.130-146del
ENST00000505433.5:c.51-46del	ENSP00000425591.1:n.51-46del
ENST00000505468.1:c.-338del	ENSP00000420886.1:n.-338del
ENST00000510761.1:c.-292-46del	ENSP00000423438.1:n.-292-46del
NM_007255.2:c.51-46del	NP_009186.1:n.51-46del
XM_005265805.2:c.-292-46del	XP_005265862.1:n.-292-46del
XM_006714816.2:c.-449-46del	XP_006714879.1:n.-449-46del
XM_011534421.1:c.-292-46del	XP_011532723.1:n.-292-46del
XM_006714816.4:c.-449-46del	XP_006714879.1:n.-449-46del
XM_017008999.2:c.-292-46del	XP_016864488.1:n.-292-46del
NM_007255.3:c.51-46del MANE Select	NP_009186.1:n.51-46del