Canonical Allele Identifier: CA2769581861

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604297del , CM000667.2:g.177604297del	GRCh38
NC_000005.9:g.177031298del , CM000667.1:g.177031298del	GRCh37
NC_000005.8:g.176963904del	NCBI36
NG_015977.1:g.9180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.169del MANE Select	ENSP00000029410.5:p.Val57TrpfsTer?
ENST00000029410.9:c.169del	ENSP00000029410.5:p.Val57TrpfsTer?
ENST00000502420.1:n.148del
ENST00000505433.5:c.169del	ENSP00000425591.1:p.Val57TrpfsTer?
ENST00000505468.1:c.-174del	ENSP00000420886.1:n.-174del
ENST00000510761.1:c.-174del	ENSP00000423438.1:n.-174del
NM_007255.2:c.169del	NP_009186.1:p.Val57TrpfsTer?
XM_005265805.2:c.-174del	XP_005265862.1:n.-174del
XM_006714816.2:c.-331del	XP_006714879.1:n.-331del
XM_011534421.1:c.-174del	XP_011532723.1:n.-174del
XM_006714816.4:c.-331del	XP_006714879.1:n.-331del
XM_017008999.2:c.-174del	XP_016864488.1:n.-174del
NM_007255.3:c.169del MANE Select	NP_009186.1:p.Val57TrpfsTer?