Canonical Allele Identifier: CA1603730385
Gene: B4GALT7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604397G= , CM000667.2:g.177604397G= GRCh38
NC_000005.9:g.177031398G= , CM000667.1:g.177031398G= GRCh37
NC_000005.8:g.176964004G= NCBI36
NG_015977.1:g.9280G=

Transcript Alleles

HGVS Amino-acid change
ENST00000029410.10:c.269G= MANE Select ENSP00000029410.5:p.Trp90=
ENST00000029410.9:c.269G= ENSP00000029410.5:p.Trp90=
ENST00000502420.1:n.248G=
ENST00000505433.5:c.269G= ENSP00000425591.1:p.Trp90=
ENST00000505468.1:c.-74G= ENSP00000420886.1:n.-74G=
ENST00000507061.1:c.86G= ENSP00000423868.1:p.Trp29=
ENST00000510761.1:c.-74G= ENSP00000423438.1:n.-74G=
NM_007255.2:c.269G= NP_009186.1:p.Trp90=
XM_005265805.2:c.-74G= XP_005265862.1:n.-74G=
XM_006714816.2:c.-231G= XP_006714879.1:n.-231G=
XM_011534421.1:c.-74G= XP_011532723.1:n.-74G=
XM_006714816.4:c.-231G= XP_006714879.1:n.-231G=
XM_017008999.2:c.-74G= XP_016864488.1:n.-74G=
NM_007255.3:c.269G= MANE Select NP_009186.1:p.Trp90=