Canonical Allele Identifier: CA1603686030

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609194_177609203delinsCTGGGCACTG , CM000667.2:g.177609194_177609203delinsCTGGGCACTG	GRCh38
NC_000005.9:g.177036195_177036204delinsCTGGGCACTG , CM000667.1:g.177036195_177036204delinsCTGGGCACTG	GRCh37
NC_000005.8:g.176968801_176968810delinsCTGGGCACTG	NCBI36
NG_015977.1:g.14077_14086delinsCTGGGCACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+180_828+189delinsCTGGGCACTG MANE Select	ENSP00000029410.5:n.828+180_828+189delinsCTGGGCACTG
ENST00000029410.9:c.828+180_828+189delinsCTGGGCACTG	ENSP00000029410.5:n.828+180_828+189delinsCTGGGCACTG
ENST00000505145.1:n.1926+180_1926+189delinsCTGGGCACTG
ENST00000505433.5:c.*334+180_*334+189delinsCTGGGCACTG	ENSP00000425591.1:n.*334+180_*334+189delinsCTGGGCACTG
ENST00000515353.1:n.1650+180_1650+189delinsCTGGGCACTG
NM_007255.2:c.828+180_828+189delinsCTGGGCACTG	NP_009186.1:n.828+180_828+189delinsCTGGGCACTG
XM_005265805.2:c.486+180_486+189delinsCTGGGCACTG	XP_005265862.1:n.486+180_486+189delinsCTGGGCACTG
XM_006714816.2:c.348+180_348+189delinsCTGGGCACTG	XP_006714879.1:n.348+180_348+189delinsCTGGGCACTG
XM_011534421.1:c.486+180_486+189delinsCTGGGCACTG	XP_011532723.1:n.486+180_486+189delinsCTGGGCACTG
XM_006714816.4:c.348+180_348+189delinsCTGGGCACTG	XP_006714879.1:n.348+180_348+189delinsCTGGGCACTG
XM_017008999.2:c.486+180_486+189delinsCTGGGCACTG	XP_016864488.1:n.486+180_486+189delinsCTGGGCACTG
NM_007255.3:c.828+180_828+189delinsCTGGGCACTG MANE Select	NP_009186.1:n.828+180_828+189delinsCTGGGCACTG