Canonical Allele Identifier: CA1603686007

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609188_177609190delinsGGC , CM000667.2:g.177609188_177609190delinsGGC	GRCh38
NC_000005.9:g.177036189_177036191delinsGGC , CM000667.1:g.177036189_177036191delinsGGC	GRCh37
NC_000005.8:g.176968795_176968797delinsGGC	NCBI36
NG_015977.1:g.14071_14073delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+174_828+176delinsGGC MANE Select	ENSP00000029410.5:n.828+174_828+176delinsGGC
ENST00000029410.9:c.828+174_828+176delinsGGC	ENSP00000029410.5:n.828+174_828+176delinsGGC
ENST00000505145.1:n.1926+174_1926+176delinsGGC
ENST00000505433.5:c.*334+174_*334+176delinsGGC	ENSP00000425591.1:n.*334+174_*334+176delinsGGC
ENST00000515353.1:n.1650+174_1650+176delinsGGC
NM_007255.2:c.828+174_828+176delinsGGC	NP_009186.1:n.828+174_828+176delinsGGC
XM_005265805.2:c.486+174_486+176delinsGGC	XP_005265862.1:n.486+174_486+176delinsGGC
XM_006714816.2:c.348+174_348+176delinsGGC	XP_006714879.1:n.348+174_348+176delinsGGC
XM_011534421.1:c.486+174_486+176delinsGGC	XP_011532723.1:n.486+174_486+176delinsGGC
XM_006714816.4:c.348+174_348+176delinsGGC	XP_006714879.1:n.348+174_348+176delinsGGC
XM_017008999.2:c.486+174_486+176delinsGGC	XP_016864488.1:n.486+174_486+176delinsGGC
NM_007255.3:c.828+174_828+176delinsGGC MANE Select	NP_009186.1:n.828+174_828+176delinsGGC