Canonical Allele Identifier: CA2676759685

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177609042-A-ACTG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609042_177609043insCTG , CM000667.2:g.177609042_177609043insCTG	GRCh38
NC_000005.9:g.177036043_177036044insCTG , CM000667.1:g.177036043_177036044insCTG	GRCh37
NC_000005.8:g.176968649_176968650insCTG	NCBI36
NG_015977.1:g.13925_13926insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+28_828+29insCTG MANE Select	ENSP00000029410.5:n.828+28_828+29insCTG
ENST00000029410.9:c.828+28_828+29insCTG	ENSP00000029410.5:n.828+28_828+29insCTG
ENST00000505145.1:n.1926+28_1926+29insCTG
ENST00000505433.5:c.*334+28_*334+29insCTG	ENSP00000425591.1:n.*334+28_*334+29insCTG
ENST00000515353.1:n.1650+28_1650+29insCTG
NM_007255.2:c.828+28_828+29insCTG	NP_009186.1:n.828+28_828+29insCTG
XM_005265805.2:c.486+28_486+29insCTG	XP_005265862.1:n.486+28_486+29insCTG
XM_006714816.2:c.348+28_348+29insCTG	XP_006714879.1:n.348+28_348+29insCTG
XM_011534421.1:c.486+28_486+29insCTG	XP_011532723.1:n.486+28_486+29insCTG
XM_006714816.4:c.348+28_348+29insCTG	XP_006714879.1:n.348+28_348+29insCTG
XM_017008999.2:c.486+28_486+29insCTG	XP_016864488.1:n.486+28_486+29insCTG
NM_007255.3:c.828+28_828+29insCTG MANE Select	NP_009186.1:n.828+28_828+29insCTG