Canonical Allele Identifier: CA2676746474

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177603970-GGTGGCATGGGTTGGGTCTAGAGAGGCAAGCAGGATTCGGATGCATGGTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177603979_177604027del , CM000667.2:g.177603979_177604027del	GRCh38
NC_000005.9:g.177030980_177031028del , CM000667.1:g.177030980_177031028del	GRCh37
NC_000005.8:g.176963586_176963634del	NCBI36
NG_015977.1:g.8862_8910del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.51-200_51-152del MANE Select	ENSP00000029410.5:n.51-200_51-152del
ENST00000029410.9:c.51-200_51-152del	ENSP00000029410.5:n.51-200_51-152del
ENST00000502420.1:n.130-300_130-252del
ENST00000505433.5:c.51-200_51-152del	ENSP00000425591.1:n.51-200_51-152del
ENST00000505468.1:c.-405-87_-405-39del	ENSP00000420886.1:n.-405-87_-405-39del
ENST00000510761.1:c.-292-200_-292-152del	ENSP00000423438.1:n.-292-200_-292-152del
NM_007255.2:c.51-200_51-152del	NP_009186.1:n.51-200_51-152del
XM_005265805.2:c.-292-200_-292-152del	XP_005265862.1:n.-292-200_-292-152del
XM_006714816.2:c.-449-200_-449-152del	XP_006714879.1:n.-449-200_-449-152del
XM_011534421.1:c.-292-200_-292-152del	XP_011532723.1:n.-292-200_-292-152del
XM_006714816.4:c.-449-200_-449-152del	XP_006714879.1:n.-449-200_-449-152del
XM_017008999.2:c.-292-200_-292-152del	XP_016864488.1:n.-292-200_-292-152del
NM_007255.3:c.51-200_51-152del MANE Select	NP_009186.1:n.51-200_51-152del