Canonical Allele Identifier: CA447984346

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177604497-G-A
• MyVariant Identifiers: chr5:g.177031498G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604497G>A , CM000667.2:g.177604497G>A	GRCh38
NC_000005.9:g.177031498G>A , CM000667.1:g.177031498G>A	GRCh37
NC_000005.8:g.176964104G>A	NCBI36
NG_015977.1:g.9380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.369G>A MANE Select	ENSP00000029410.5:p.Lys123=
ENST00000029410.9:c.369G>A	ENSP00000029410.5:p.Lys123=
ENST00000502420.1:n.348G>A
ENST00000505433.5:c.369G>A	ENSP00000425591.1:p.Lys123=
ENST00000505468.1:c.27G>A	ENSP00000420886.1:p.Lys9=
ENST00000507061.1:c.186G>A	ENSP00000423868.1:p.Lys62=
ENST00000510761.1:c.27G>A	ENSP00000423438.1:p.Lys9=
NM_007255.2:c.369G>A	NP_009186.1:p.Lys123=
XM_005265805.2:c.27G>A	XP_005265862.1:p.Lys9=
XM_006714816.2:c.-131G>A	XP_006714879.1:n.-131G>A
XM_011534421.1:c.27G>A	XP_011532723.1:p.Lys9=
XM_006714816.4:c.-131G>A	XP_006714879.1:n.-131G>A
XM_017008999.2:c.27G>A	XP_016864488.1:p.Lys9=
NM_007255.3:c.369G>A MANE Select	NP_009186.1:p.Lys123=