Canonical Allele Identifier: CA2578500141

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608813del , CM000667.2:g.177608813del	GRCh38
NC_000005.9:g.177035814del , CM000667.1:g.177035814del	GRCh37
NC_000005.8:g.176968420del	NCBI36
NG_015977.1:g.13696del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-97del MANE Select	ENSP00000029410.5:n.724-97del
ENST00000029410.9:c.724-97del	ENSP00000029410.5:n.724-97del
ENST00000505145.1:n.1822-97del
ENST00000505433.5:c.*230-97del	ENSP00000425591.1:n.*230-97del
ENST00000515353.1:n.1449del
NM_007255.2:c.724-97del	NP_009186.1:n.724-97del
XM_005265805.2:c.382-97del	XP_005265862.1:n.382-97del
XM_006714816.2:c.244-97del	XP_006714879.1:n.244-97del
XM_011534421.1:c.382-97del	XP_011532723.1:n.382-97del
XM_006714816.4:c.244-97del	XP_006714879.1:n.244-97del
XM_017008999.2:c.382-97del	XP_016864488.1:n.382-97del
NM_007255.3:c.724-97del MANE Select	NP_009186.1:n.724-97del