Canonical Allele Identifier: CA2578500120

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608653-AGCTGCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608655_177608660del , CM000667.2:g.177608655_177608660del	GRCh38
NC_000005.9:g.177035656_177035661del , CM000667.1:g.177035656_177035661del	GRCh37
NC_000005.8:g.176968262_176968267del	NCBI36
NG_015977.1:g.13538_13543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+33_723+38del MANE Select	ENSP00000029410.5:n.723+33_723+38del
ENST00000029410.9:c.723+33_723+38del	ENSP00000029410.5:n.723+33_723+38del
ENST00000505145.1:n.1821+33_1821+38del
ENST00000505433.5:c.*229+33_*229+38del	ENSP00000425591.1:n.*229+33_*229+38del
ENST00000515353.1:n.1291_1296del
NM_007255.2:c.723+33_723+38del	NP_009186.1:n.723+33_723+38del
XM_005265805.2:c.381+33_381+38del	XP_005265862.1:n.381+33_381+38del
XM_006714816.2:c.243+33_243+38del	XP_006714879.1:n.243+33_243+38del
XM_011534421.1:c.381+33_381+38del	XP_011532723.1:n.381+33_381+38del
XM_006714816.4:c.243+33_243+38del	XP_006714879.1:n.243+33_243+38del
XM_017008999.2:c.381+33_381+38del	XP_016864488.1:n.381+33_381+38del
NM_007255.3:c.723+33_723+38del MANE Select	NP_009186.1:n.723+33_723+38del