Canonical Allele Identifier: CA1603676076
Gene: B4GALT7 HGNC NCBI

Linked Data

dbSNP Id: rs1767934356

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604627_177604632dup , CM000667.2:g.177604627_177604632dup GRCh38
NC_000005.9:g.177031628_177031633dup , CM000667.1:g.177031628_177031633dup GRCh37
NC_000005.8:g.176964234_176964239dup NCBI36
NG_015977.1:g.9510_9515dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000029410.10:c.413+86_413+91dup MANE Select ENSP00000029410.5:n.413+86_413+91dup
ENST00000029410.9:c.413+86_413+91dup ENSP00000029410.5:n.413+86_413+91dup
ENST00000502420.1:n.392+86_392+91dup
ENST00000505433.5:c.413+86_413+91dup ENSP00000425591.1:n.413+86_413+91dup
ENST00000505468.1:c.71+86_71+91dup ENSP00000420886.1:n.71+86_71+91dup
ENST00000507061.1:c.230+86_230+91dup ENSP00000423868.1:n.230+86_230+91dup
ENST00000510761.1:c.71+86_71+91dup ENSP00000423438.1:n.71+86_71+91dup
NM_007255.2:c.413+86_413+91dup NP_009186.1:n.413+86_413+91dup
XM_005265805.2:c.71+86_71+91dup XP_005265862.1:n.71+86_71+91dup
XM_006714816.2:c.-87+86_-87+91dup XP_006714879.1:n.-87+86_-87+91dup
XM_011534421.1:c.71+86_71+91dup XP_011532723.1:n.71+86_71+91dup
XM_006714816.4:c.-87+86_-87+91dup XP_006714879.1:n.-87+86_-87+91dup
XM_017008999.2:c.71+86_71+91dup XP_016864488.1:n.71+86_71+91dup
NM_007255.3:c.413+86_413+91dup MANE Select NP_009186.1:n.413+86_413+91dup