Canonical Allele Identifier: CA2676759132
Gene: B4GALT7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177608825_177608826insACAGGAAGGGACC , CM000667.2:g.177608825_177608826insACAGGAAGGGACC GRCh38
NC_000005.9:g.177035826_177035827insACAGGAAGGGACC , CM000667.1:g.177035826_177035827insACAGGAAGGGACC GRCh37
NC_000005.8:g.176968432_176968433insACAGGAAGGGACC NCBI36
NG_015977.1:g.13708_13709insACAGGAAGGGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000029410.10:c.724-85_724-84insACAGGAAGGGACC MANE Select ENSP00000029410.5:n.724-85_724-84insACAGGAAGGGACC
ENST00000029410.9:c.724-85_724-84insACAGGAAGGGACC ENSP00000029410.5:n.724-85_724-84insACAGGAAGGGACC
ENST00000505145.1:n.1822-85_1822-84insACAGGAAGGGACC
ENST00000505433.5:c.*230-85_*230-84insACAGGAAGGGACC ENSP00000425591.1:n.*230-85_*230-84insACAGGAAGGGACC
ENST00000515353.1:n.1461_1462insACAGGAAGGGACC
NM_007255.2:c.724-85_724-84insACAGGAAGGGACC NP_009186.1:n.724-85_724-84insACAGGAAGGGACC
XM_005265805.2:c.382-85_382-84insACAGGAAGGGACC XP_005265862.1:n.382-85_382-84insACAGGAAGGGACC
XM_006714816.2:c.244-85_244-84insACAGGAAGGGACC XP_006714879.1:n.244-85_244-84insACAGGAAGGGACC
XM_011534421.1:c.382-85_382-84insACAGGAAGGGACC XP_011532723.1:n.382-85_382-84insACAGGAAGGGACC
XM_006714816.4:c.244-85_244-84insACAGGAAGGGACC XP_006714879.1:n.244-85_244-84insACAGGAAGGGACC
XM_017008999.2:c.382-85_382-84insACAGGAAGGGACC XP_016864488.1:n.382-85_382-84insACAGGAAGGGACC
NM_007255.3:c.724-85_724-84insACAGGAAGGGACC MANE Select NP_009186.1:n.724-85_724-84insACAGGAAGGGACC