Canonical Allele Identifier: CA2676746602

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177604040-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604040A>G , CM000667.2:g.177604040A>G	GRCh38
NC_000005.9:g.177031041A>G , CM000667.1:g.177031041A>G	GRCh37
NC_000005.8:g.176963647A>G	NCBI36
NG_015977.1:g.8923A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.51-139A>G MANE Select	ENSP00000029410.5:n.51-139A>G
ENST00000029410.9:c.51-139A>G	ENSP00000029410.5:n.51-139A>G
ENST00000502420.1:n.130-239A>G
ENST00000505433.5:c.51-139A>G	ENSP00000425591.1:n.51-139A>G
ENST00000505468.1:c.-405-26A>G	ENSP00000420886.1:n.-405-26A>G
ENST00000510761.1:c.-292-139A>G	ENSP00000423438.1:n.-292-139A>G
NM_007255.2:c.51-139A>G	NP_009186.1:n.51-139A>G
XM_005265805.2:c.-292-139A>G	XP_005265862.1:n.-292-139A>G
XM_006714816.2:c.-449-139A>G	XP_006714879.1:n.-449-139A>G
XM_011534421.1:c.-292-139A>G	XP_011532723.1:n.-292-139A>G
XM_006714816.4:c.-449-139A>G	XP_006714879.1:n.-449-139A>G
XM_017008999.2:c.-292-139A>G	XP_016864488.1:n.-292-139A>G
NM_007255.3:c.51-139A>G MANE Select	NP_009186.1:n.51-139A>G