Canonical Allele Identifier: CA1603686042

Gene: B4GALT7

Linked Data

• dbSNP Id: rs1768106156

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609198del , CM000667.2:g.177609198del	GRCh38
NC_000005.9:g.177036199del , CM000667.1:g.177036199del	GRCh37
NC_000005.8:g.176968805del	NCBI36
NG_015977.1:g.14081del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+184del MANE Select	ENSP00000029410.5:n.828+184del
ENST00000029410.9:c.828+184del	ENSP00000029410.5:n.828+184del
ENST00000505145.1:n.1926+184del
ENST00000505433.5:c.*334+184del	ENSP00000425591.1:n.*334+184del
ENST00000515353.1:n.1650+184del
NM_007255.2:c.828+184del	NP_009186.1:n.828+184del
XM_005265805.2:c.486+184del	XP_005265862.1:n.486+184del
XM_006714816.2:c.348+184del	XP_006714879.1:n.348+184del
XM_011534421.1:c.486+184del	XP_011532723.1:n.486+184del
XM_006714816.4:c.348+184del	XP_006714879.1:n.348+184del
XM_017008999.2:c.486+184del	XP_016864488.1:n.486+184del
NM_007255.3:c.828+184del MANE Select	NP_009186.1:n.828+184del