Canonical Allele Identifier: CA2769581862

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604300del , CM000667.2:g.177604300del	GRCh38
NC_000005.9:g.177031301del , CM000667.1:g.177031301del	GRCh37
NC_000005.8:g.176963907del	NCBI36
NG_015977.1:g.9183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.172del MANE Select	ENSP00000029410.5:p.Ala58ProfsTer?
ENST00000029410.9:c.172del	ENSP00000029410.5:p.Ala58ProfsTer?
ENST00000502420.1:n.151del
ENST00000505433.5:c.172del	ENSP00000425591.1:p.Ala58ProfsTer?
ENST00000505468.1:c.-171del	ENSP00000420886.1:n.-171del
ENST00000510761.1:c.-171del	ENSP00000423438.1:n.-171del
NM_007255.2:c.172del	NP_009186.1:p.Ala58ProfsTer?
XM_005265805.2:c.-171del	XP_005265862.1:n.-171del
XM_006714816.2:c.-328del	XP_006714879.1:n.-328del
XM_011534421.1:c.-171del	XP_011532723.1:n.-171del
XM_006714816.4:c.-328del	XP_006714879.1:n.-328del
XM_017008999.2:c.-171del	XP_016864488.1:n.-171del
NM_007255.3:c.172del MANE Select	NP_009186.1:p.Ala58ProfsTer?