Canonical Allele Identifier: CA1603684941

Gene: B4GALT7

Linked Data

• dbSNP Id: rs1768091455

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608786_177608787del , CM000667.2:g.177608786_177608787del	GRCh38
NC_000005.9:g.177035787_177035788del , CM000667.1:g.177035787_177035788del	GRCh37
NC_000005.8:g.176968393_176968394del	NCBI36
NG_015977.1:g.13669_13670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-124_724-123del MANE Select	ENSP00000029410.5:n.724-124_724-123del
ENST00000029410.9:c.724-124_724-123del	ENSP00000029410.5:n.724-124_724-123del
ENST00000505145.1:n.1822-124_1822-123del
ENST00000505433.5:c.*230-124_*230-123del	ENSP00000425591.1:n.*230-124_*230-123del
ENST00000515353.1:n.1422_1423del
NM_007255.2:c.724-124_724-123del	NP_009186.1:n.724-124_724-123del
XM_005265805.2:c.382-124_382-123del	XP_005265862.1:n.382-124_382-123del
XM_006714816.2:c.244-124_244-123del	XP_006714879.1:n.244-124_244-123del
XM_011534421.1:c.382-124_382-123del	XP_011532723.1:n.382-124_382-123del
XM_006714816.4:c.244-124_244-123del	XP_006714879.1:n.244-124_244-123del
XM_017008999.2:c.382-124_382-123del	XP_016864488.1:n.382-124_382-123del
NM_007255.3:c.724-124_724-123del MANE Select	NP_009186.1:n.724-124_724-123del