Canonical Allele Identifier: CA2505021315

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608695-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608696dup , CM000667.2:g.177608696dup	GRCh38
NC_000005.9:g.177035697dup , CM000667.1:g.177035697dup	GRCh37
NC_000005.8:g.176968303dup	NCBI36
NG_015977.1:g.13579dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+74dup MANE Select	ENSP00000029410.5:n.723+74dup
ENST00000029410.9:c.723+74dup	ENSP00000029410.5:n.723+74dup
ENST00000505145.1:n.1821+74dup
ENST00000505433.5:c.*229+74dup	ENSP00000425591.1:n.*229+74dup
ENST00000515353.1:n.1332dup
NM_007255.2:c.723+74dup	NP_009186.1:n.723+74dup
XM_005265805.2:c.381+74dup	XP_005265862.1:n.381+74dup
XM_006714816.2:c.243+74dup	XP_006714879.1:n.243+74dup
XM_011534421.1:c.381+74dup	XP_011532723.1:n.381+74dup
XM_006714816.4:c.243+74dup	XP_006714879.1:n.243+74dup
XM_017008999.2:c.381+74dup	XP_016864488.1:n.381+74dup
NM_007255.3:c.723+74dup MANE Select	NP_009186.1:n.723+74dup