Canonical Allele Identifier: CA2676758938

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608743-ACCCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608750_177608754del , CM000667.2:g.177608750_177608754del	GRCh38
NC_000005.9:g.177035751_177035755del , CM000667.1:g.177035751_177035755del	GRCh37
NC_000005.8:g.176968357_176968361del	NCBI36
NG_015977.1:g.13633_13637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+128_723+132del MANE Select	ENSP00000029410.5:n.723+128_723+132del
ENST00000029410.9:c.723+128_723+132del	ENSP00000029410.5:n.723+128_723+132del
ENST00000505145.1:n.1821+128_1821+132del
ENST00000505433.5:c.*229+128_*229+132del	ENSP00000425591.1:n.*229+128_*229+132del
ENST00000515353.1:n.1386_1390del
NM_007255.2:c.723+128_723+132del	NP_009186.1:n.723+128_723+132del
XM_005265805.2:c.381+128_381+132del	XP_005265862.1:n.381+128_381+132del
XM_006714816.2:c.243+128_243+132del	XP_006714879.1:n.243+128_243+132del
XM_011534421.1:c.381+128_381+132del	XP_011532723.1:n.381+128_381+132del
XM_006714816.4:c.243+128_243+132del	XP_006714879.1:n.243+128_243+132del
XM_017008999.2:c.381+128_381+132del	XP_016864488.1:n.381+128_381+132del
NM_007255.3:c.723+128_723+132del MANE Select	NP_009186.1:n.723+128_723+132del