Canonical Allele Identifier: CA1603730322
Gene: B4GALT7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604303C= , CM000667.2:g.177604303C= GRCh38
NC_000005.9:g.177031304C= , CM000667.1:g.177031304C= GRCh37
NC_000005.8:g.176963910C= NCBI36
NG_015977.1:g.9186C=

Transcript Alleles

HGVS Amino-acid change
ENST00000029410.10:c.175C= MANE Select ENSP00000029410.5:p.Arg59=
ENST00000029410.9:c.175C= ENSP00000029410.5:p.Arg59=
ENST00000502420.1:n.154C=
ENST00000505433.5:c.175C= ENSP00000425591.1:p.Arg59=
ENST00000505468.1:c.-168C= ENSP00000420886.1:n.-168C=
ENST00000510761.1:c.-168C= ENSP00000423438.1:n.-168C=
NM_007255.2:c.175C= NP_009186.1:p.Arg59=
XM_005265805.2:c.-168C= XP_005265862.1:n.-168C=
XM_006714816.2:c.-325C= XP_006714879.1:n.-325C=
XM_011534421.1:c.-168C= XP_011532723.1:n.-168C=
XM_006714816.4:c.-325C= XP_006714879.1:n.-325C=
XM_017008999.2:c.-168C= XP_016864488.1:n.-168C=
NM_007255.3:c.175C= MANE Select NP_009186.1:p.Arg59=