Canonical Allele Identifier: CA132896518

Gene: B4GALT7

Linked Data

• dbSNP Id: rs1035241186
• gnomAD v2: 5-177035782-TG-T
• gnomAD v3: 5-177608781-TG-T
• gnomAD v4: 5-177608781-TG-T
• MyVariant Identifiers: chr5:g.177035783del (hg19) ; chr5:g.177608782del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608782del , CM000667.2:g.177608782del	GRCh38
NC_000005.9:g.177035783del , CM000667.1:g.177035783del	GRCh37
NC_000005.8:g.176968389del	NCBI36
NG_015977.1:g.13665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-128del MANE Select	ENSP00000029410.5:n.724-128del
ENST00000029410.9:c.724-128del	ENSP00000029410.5:n.724-128del
ENST00000505145.1:n.1822-128del
ENST00000505433.5:c.*230-128del	ENSP00000425591.1:n.*230-128del
ENST00000515353.1:n.1418del
NM_007255.2:c.724-128del	NP_009186.1:n.724-128del
XM_005265805.2:c.382-128del	XP_005265862.1:n.382-128del
XM_006714816.2:c.244-128del	XP_006714879.1:n.244-128del
XM_011534421.1:c.382-128del	XP_011532723.1:n.382-128del
XM_006714816.4:c.244-128del	XP_006714879.1:n.244-128del
XM_017008999.2:c.382-128del	XP_016864488.1:n.382-128del
NM_007255.3:c.724-128del MANE Select	NP_009186.1:n.724-128del