Canonical Allele Identifier: CA2676759134

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608825-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608826_177608827del , CM000667.2:g.177608826_177608827del	GRCh38
NC_000005.9:g.177035827_177035828del , CM000667.1:g.177035827_177035828del	GRCh37
NC_000005.8:g.176968433_176968434del	NCBI36
NG_015977.1:g.13709_13710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-84_724-83del MANE Select	ENSP00000029410.5:n.724-84_724-83del
ENST00000029410.9:c.724-84_724-83del	ENSP00000029410.5:n.724-84_724-83del
ENST00000505145.1:n.1822-84_1822-83del
ENST00000505433.5:c.*230-84_*230-83del	ENSP00000425591.1:n.*230-84_*230-83del
ENST00000515353.1:n.1462_1463del
NM_007255.2:c.724-84_724-83del	NP_009186.1:n.724-84_724-83del
XM_005265805.2:c.382-84_382-83del	XP_005265862.1:n.382-84_382-83del
XM_006714816.2:c.244-84_244-83del	XP_006714879.1:n.244-84_244-83del
XM_011534421.1:c.382-84_382-83del	XP_011532723.1:n.382-84_382-83del
XM_006714816.4:c.244-84_244-83del	XP_006714879.1:n.244-84_244-83del
XM_017008999.2:c.382-84_382-83del	XP_016864488.1:n.382-84_382-83del
NM_007255.3:c.724-84_724-83del MANE Select	NP_009186.1:n.724-84_724-83del