Canonical Allele Identifier: CA2606576204

Gene: B4GALT7

Linked Data

• gnomAD v3: 5-177608686-TTCC-T
• gnomAD v4: 5-177608686-TTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608689_177608691del , CM000667.2:g.177608689_177608691del	GRCh38
NC_000005.9:g.177035690_177035692del , CM000667.1:g.177035690_177035692del	GRCh37
NC_000005.8:g.176968296_176968298del	NCBI36
NG_015977.1:g.13572_13574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+67_723+69del MANE Select	ENSP00000029410.5:n.723+67_723+69del
ENST00000029410.9:c.723+67_723+69del	ENSP00000029410.5:n.723+67_723+69del
ENST00000505145.1:n.1821+67_1821+69del
ENST00000505433.5:c.*229+67_*229+69del	ENSP00000425591.1:n.*229+67_*229+69del
ENST00000515353.1:n.1325_1327del
NM_007255.2:c.723+67_723+69del	NP_009186.1:n.723+67_723+69del
XM_005265805.2:c.381+67_381+69del	XP_005265862.1:n.381+67_381+69del
XM_006714816.2:c.243+67_243+69del	XP_006714879.1:n.243+67_243+69del
XM_011534421.1:c.381+67_381+69del	XP_011532723.1:n.381+67_381+69del
XM_006714816.4:c.243+67_243+69del	XP_006714879.1:n.243+67_243+69del
XM_017008999.2:c.381+67_381+69del	XP_016864488.1:n.381+67_381+69del
NM_007255.3:c.723+67_723+69del MANE Select	NP_009186.1:n.723+67_723+69del