Canonical Allele Identifier: CA2676759244

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608886-C-CCCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608888_177608891dup , CM000667.2:g.177608888_177608891dup	GRCh38
NC_000005.9:g.177035889_177035892dup , CM000667.1:g.177035889_177035892dup	GRCh37
NC_000005.8:g.176968495_176968498dup	NCBI36
NG_015977.1:g.13771_13774dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-22_724-19dup MANE Select	ENSP00000029410.5:n.724-22_724-19dup
ENST00000029410.9:c.724-22_724-19dup	ENSP00000029410.5:n.724-22_724-19dup
ENST00000505145.1:n.1822-22_1822-19dup
ENST00000505433.5:c.*230-22_*230-19dup	ENSP00000425591.1:n.*230-22_*230-19dup
ENST00000515353.1:n.1524_1527dup
NM_007255.2:c.724-22_724-19dup	NP_009186.1:n.724-22_724-19dup
XM_005265805.2:c.382-22_382-19dup	XP_005265862.1:n.382-22_382-19dup
XM_006714816.2:c.244-22_244-19dup	XP_006714879.1:n.244-22_244-19dup
XM_011534421.1:c.382-22_382-19dup	XP_011532723.1:n.382-22_382-19dup
XM_006714816.4:c.244-22_244-19dup	XP_006714879.1:n.244-22_244-19dup
XM_017008999.2:c.382-22_382-19dup	XP_016864488.1:n.382-22_382-19dup
NM_007255.3:c.724-22_724-19dup MANE Select	NP_009186.1:n.724-22_724-19dup