Canonical Allele Identifier: CA1603730394
Gene: B4GALT7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604405C= , CM000667.2:g.177604405C= GRCh38
NC_000005.9:g.177031406C= , CM000667.1:g.177031406C= GRCh37
NC_000005.8:g.176964012C= NCBI36
NG_015977.1:g.9288C=

Transcript Alleles

HGVS Amino-acid change
ENST00000029410.10:c.277C= MANE Select ENSP00000029410.5:p.His93=
ENST00000029410.9:c.277C= ENSP00000029410.5:p.His93=
ENST00000502420.1:n.256C=
ENST00000505433.5:c.277C= ENSP00000425591.1:p.His93=
ENST00000505468.1:c.-66C= ENSP00000420886.1:n.-66C=
ENST00000507061.1:c.94C= ENSP00000423868.1:p.His32=
ENST00000510761.1:c.-66C= ENSP00000423438.1:n.-66C=
NM_007255.2:c.277C= NP_009186.1:p.His93=
XM_005265805.2:c.-66C= XP_005265862.1:n.-66C=
XM_006714816.2:c.-223C= XP_006714879.1:n.-223C=
XM_011534421.1:c.-66C= XP_011532723.1:n.-66C=
XM_006714816.4:c.-223C= XP_006714879.1:n.-223C=
XM_017008999.2:c.-66C= XP_016864488.1:n.-66C=
NM_007255.3:c.277C= MANE Select NP_009186.1:p.His93=