Canonical Allele Identifier: CA2676758994

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608759-T-TTAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608759_177608760insTAGGG , CM000667.2:g.177608759_177608760insTAGGG	GRCh38
NC_000005.9:g.177035760_177035761insTAGGG , CM000667.1:g.177035760_177035761insTAGGG	GRCh37
NC_000005.8:g.176968366_176968367insTAGGG	NCBI36
NG_015977.1:g.13642_13643insTAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+137_723+138insTAGGG MANE Select	ENSP00000029410.5:n.723+137_723+138insTAGGG
ENST00000029410.9:c.723+137_723+138insTAGGG	ENSP00000029410.5:n.723+137_723+138insTAGGG
ENST00000505145.1:n.1821+137_1821+138insTAGGG
ENST00000505433.5:c.*229+137_*229+138insTAGGG	ENSP00000425591.1:n.*229+137_*229+138insTAGGG
ENST00000515353.1:n.1395_1396insTAGGG
NM_007255.2:c.723+137_723+138insTAGGG	NP_009186.1:n.723+137_723+138insTAGGG
XM_005265805.2:c.381+137_381+138insTAGGG	XP_005265862.1:n.381+137_381+138insTAGGG
XM_006714816.2:c.243+137_243+138insTAGGG	XP_006714879.1:n.243+137_243+138insTAGGG
XM_011534421.1:c.381+137_381+138insTAGGG	XP_011532723.1:n.381+137_381+138insTAGGG
XM_006714816.4:c.243+137_243+138insTAGGG	XP_006714879.1:n.243+137_243+138insTAGGG
XM_017008999.2:c.381+137_381+138insTAGGG	XP_016864488.1:n.381+137_381+138insTAGGG
NM_007255.3:c.723+137_723+138insTAGGG MANE Select	NP_009186.1:n.723+137_723+138insTAGGG